×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
CausalMutation
disease
CLINVAR
Diagnosing childhood-onset inborn errors of metabolism by next-generation sequencing.
28468868
2017
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
Biomarker
disease
GENOMICS_ENGLAND
Severe early onset retinitis pigmentosa in a Moroccan patient with Heimler syndrome due to novel homozygous mutation of PEX1 gene.
27633571
2016
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
CausalMutation
disease
CLINVAR
Dysmorphic Facial Features and Other Clinical Characteristics in Two Patients with PEX1 Gene Mutations.
27882258
2016
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
Biomarker
disease
GENOMICS_ENGLAND
Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes.
27604308
2016
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
CausalMutation
disease
CLINVAR
Friedreich Ataxia in Classical Galactosaemia.
26219880
2016
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
CausalMutation
disease
CLINVAR
Zellweger spectrum disorders: clinical manifestations in patients surviving into adulthood.
26287655
2016
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
CausalMutation
disease
CLINVAR
Diagnosis of a mild peroxisomal phenotype with next-generation sequencing.
27872819
2016
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
CausalMutation
disease
CLINVAR
Low bone mineral density is a common feature of Zellweger spectrum disorders.
26643206
2016
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
CausalMutation
disease
CLINVAR
Zellweger syndrome with severe malnutrition, immunocompromised state and opportunistic infections.
27090541
2016
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
GeneticVariation
disease
CLINVAR
Next generation sequencing based identification of disease-associated mutations in Swiss patients with retinal dystrophies.
27353947
2016
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
GeneticVariation
disease
CLINVAR
Zellweger syndrome with severe malnutrition, immunocompromised state and opportunistic infections.
27090541
2016
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
Biomarker
disease
GENOMICS_ENGLAND
A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies.
25655951
2015
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
CausalMutation
disease
CLINVAR
Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing.
25412400
2015
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
GeneticVariation
disease
CLINVAR
RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.
25525159
2015
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
CausalMutation
disease
CLINVAR
Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6.
26387595
2015
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
GeneticVariation
disease
CLINVAR
Repository of mutations from Oman: The entry point to a national mutation database.
26594346
2015
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
CausalMutation
disease
CLINVAR
The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorder.
24503136
2014
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
CausalMutation
disease
CLINVAR
Analysis of a Chinese pedigree with Zellweger syndrome reveals a novel PEX1 mutation by next-generation sequencing.
23247051
2013
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
GeneticVariation
disease
CLINVAR
Analysis of a Chinese pedigree with Zellweger syndrome reveals a novel PEX1 mutation by next-generation sequencing.
23247051
2013
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
GeneticVariation
disease
CLINVAR
Characterization of two common 5' polymorphisms in PEX1 and correlation to survival in PEX1 peroxisome biogenesis disorder patients.
21846392
2011
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
CausalMutation
disease
CLINVAR
Characterization of two common 5' polymorphisms in PEX1 and correlation to survival in PEX1 peroxisome biogenesis disorder patients.
21846392
2011
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
GeneticVariation
disease
CLINVAR
Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorder.
21031596
2011
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
GeneticVariation
disease
CLINVAR
Two novel PEX1 mutations in a patient with Zellweger syndrome: the first Korean case confirmed by biochemical, and molecular evidence.
21844578
2011
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
CausalMutation
disease
CLINVAR
Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorder.
21031596
2011
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.600
CausalMutation
disease
CLINVAR
Germinal matrix hemorrhage in Zellweger syndrome.
20952722
2010