rs1085307550
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies.
26741492
2016
rs1085307550
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
Novel ECHS1 mutation in an Emirati neonate with severe metabolic acidosis.
27221955
2016
rs1426014295
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies.
26741492
2016
rs1426014295
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
Novel ECHS1 mutation in an Emirati neonate with severe metabolic acidosis.
27221955
2016
rs758723288
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
A
0.700
GeneticVariation
CLINVAR
A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.
26938784
2016
rs761989177
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
Novel ECHS1 mutation in an Emirati neonate with severe metabolic acidosis.
27221955
2016
rs761989177
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies.
26741492
2016
rs769429279
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies.
26741492
2016
rs769429279
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
Novel ECHS1 mutation in an Emirati neonate with severe metabolic acidosis.
27221955
2016
rs1085307550
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
ECHS1 mutations cause combined respiratory chain deficiency resulting in Leigh syndrome.
25393721
2015
rs1085307550
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
Clinical, biochemical and metabolic characterisation of a mild form of human short-chain enoyl-CoA hydratase deficiency: significance of increased N-acetyl-S-(2-carboxypropyl)cysteine excretion.
26251176
2015
rs1085307550
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement.
26000322
2015
rs1426014295
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
Clinical, biochemical and metabolic characterisation of a mild form of human short-chain enoyl-CoA hydratase deficiency: significance of increased N-acetyl-S-(2-carboxypropyl)cysteine excretion.
26251176
2015
rs1426014295
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement.
26000322
2015
rs1426014295
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
ECHS1 mutations cause combined respiratory chain deficiency resulting in Leigh syndrome.
25393721
2015
rs761989177
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement.
26000322
2015
rs761989177
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
Clinical, biochemical and metabolic characterisation of a mild form of human short-chain enoyl-CoA hydratase deficiency: significance of increased N-acetyl-S-(2-carboxypropyl)cysteine excretion.
26251176
2015
rs761989177
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
ECHS1 mutations cause combined respiratory chain deficiency resulting in Leigh syndrome.
25393721
2015
rs769429279
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement.
26000322
2015
rs769429279
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
ECHS1 mutations cause combined respiratory chain deficiency resulting in Leigh syndrome.
25393721
2015
rs769429279
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
Clinical, biochemical and metabolic characterisation of a mild form of human short-chain enoyl-CoA hydratase deficiency: significance of increased N-acetyl-S-(2-carboxypropyl)cysteine excretion.
26251176
2015
rs1085307550
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
ECHS1 mutations in Leigh disease: a new inborn error of metabolism affecting valine metabolism.
25125611
2014
rs1426014295
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
ECHS1 mutations in Leigh disease: a new inborn error of metabolism affecting valine metabolism.
25125611
2014
rs761989177
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
ECHS1 mutations in Leigh disease: a new inborn error of metabolism affecting valine metabolism.
25125611
2014
rs769429279
×
Entrez Id:
1892
Gene Symbol:
ECHS1
ECHS1
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
0.700
GeneticVariation
UNIPROT
ECHS1 mutations in Leigh disease: a new inborn error of metabolism affecting valine metabolism.
25125611
2014