×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.570
GeneticVariation
group
BEFREE
We identified a novel nonsense variant in DSG2 (c.710T > A, p.Leu237Ter ) and a reported pathogenic missense variant of distal myopathy in MYH7 (c. 1322C > T, p.Thr441Met ) in the proband of an ARVC pedigree.
31653443
2020
×
Entrez Id:
7273
Gene Symbol:
TTN
TTN
0.570
Biomarker
group
GENOMICS_ENGLAND
Mutations in the gene encoding the giant skeletal muscle protein titin are associated with a variety of muscle disorders, including recessive congenital myopathies ±cardiomyopathy, limb girdle muscular dystrophy (LGMD) and late onset dominant distal myopathy .
28716623
2017
×
Entrez Id:
7273
Gene Symbol:
TTN
TTN
0.570
GeneticVariation
group
BEFREE
Mutations in the gene encoding the giant skeletal muscle protein titin are associated with a variety of muscle disorders, including recessive congenital myopathies ±cardiomyopathy, limb girdle muscular dystrophy (LGMD) and late onset dominant distal myopathy .
28716623
2017
×
Entrez Id:
7273
Gene Symbol:
TTN
TTN
0.570
GeneticVariation
group
BEFREE
In this study, we describe a distinct phenotype for patients with distal myopathy associated with novel recessive TTN variants including a Serbian founder variant.
28295036
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.570
GeneticVariation
group
BEFREE
Myoimaging in the NGS era: the discovery of a novel mutation in MYH7 in a family with distal myopathy and core-like features--a case report.
27005958
2016
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.570
Biomarker
group
BEFREE
Novel mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7 ) distal myopathy .
24664454
2014
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.570
Biomarker
group
BEFREE
We suggest that MYH7 screening should be considered in undiagnosed late-onset distal myopathy or cytoplasmic body myopathy patients.
22521714
2012
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.570
GeneticVariation
group
BEFREE
Novel mutation in MYH7 gene associated with distal myopathy and cardiomyopathy.
21211974
2011
×
Entrez Id:
7273
Gene Symbol:
TTN
TTN
0.570
GeneticVariation
group
LHGDN
Samples from 25 new families and 25 sporadic new distal myopathy cases were screened for titin mutations.
18948003
2008
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.570
GeneticVariation
group
BEFREE
Here, we describe a unique combination of hypertrophic cardiomyopathy and hypertrophic distal myopathy in a family with a MYH7 Val606Met mutation (exon 16).
17383184
2007
×
Entrez Id:
7273
Gene Symbol:
TTN
TTN
0.570
GeneticVariation
group
BEFREE
Of these, only titin mutations were previously known to cause dominant late-onset distal myopathy .
17337483
2007
×
Entrez Id:
7273
Gene Symbol:
TTN
TTN
0.570
GeneticVariation
group
BEFREE
Mutations in titin are well known cause of late onset autosomal dominant distal myopathy .
16793270
2006
×
Entrez Id:
7273
Gene Symbol:
TTN
TTN
0.570
GeneticVariation
group
BEFREE
Titinopathies and extension of the M-line mutation phenotype beyond distal myopathy and LGMD2J .
15728284
2005
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.570
Biomarker
group
GENOMICS_ENGLAND
These findings demonstrate that heterozygous mutations toward the 3' end of MYH7 cause Laing-type early-onset distal myopathy .
15322983
2004
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.570
GeneticVariation
group
LHGDN
These findings demonstrate that heterozygous mutations toward the 3' end of MYH7 cause Laing-type early-onset distal myopathy .
15322983
2004
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.570
GeneticVariation
group
BEFREE
These findings demonstrate that heterozygous mutations toward the 3' end of MYH7 cause Laing-type early-onset distal myopathy .
15322983
2004
×
Entrez Id:
7273
Gene Symbol:
TTN
TTN
0.570
GeneticVariation
group
LHGDN
Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titin.
12145747
2002
×
Entrez Id:
7273
Gene Symbol:
TTN
TTN
0.570
Biomarker
group
CTD_human
Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titin.
12145747
2002
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.570
Biomarker
group
CTD_human
×
Entrez Id:
26353
Gene Symbol:
HSPB8
HSPB8
0.420
GeneticVariation
group
CLINVAR
Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy.
29029362
2018
×
Entrez Id:
26353
Gene Symbol:
HSPB8
HSPB8
0.420
Biomarker
group
BEFREE
Mutations in the small heat shock protein B8 gene (HSPB8/HSP22 ) have been associated with distal hereditary motor neuropathy, Charcot-Marie-Tooth disease, and recently distal myopathy .
28780615
2018
×
Entrez Id:
26353
Gene Symbol:
HSPB8
HSPB8
0.420
GeneticVariation
group
CLINVAR
HSPB8 haploinsufficiency causes dominant adult-onset axial and distal myopathy.
28501893
2017
×
Entrez Id:
26353
Gene Symbol:
HSPB8
HSPB8
0.420
GeneticVariation
group
BEFREE
Mutations in HSPB8 causing a new phenotype of distal myopathy and motor neuropathy.
26718575
2016
×
Entrez Id:
26353
Gene Symbol:
HSPB8
HSPB8
0.420
Biomarker
group
GENOMICS_ENGLAND
Mutations in HSPB8 causing a new phenotype of distal myopathy and motor neuropathy.
26718575
2016
×
Entrez Id:
26353
Gene Symbol:
HSPB8
HSPB8
0.420
GeneticVariation
group
CLINVAR
Mutations in HSPB8 causing a new phenotype of distal myopathy and motor neuropathy.
26976520
2016