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Article

A feline orthologue of the human MYH7 c.5647G>A (p.(Glu1883Lys)) variant causes hypertrophic cardiomyopathy in a Domestic Shorthair cat

4 Jun 2019

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 31164718
DOI: 10.1038/s41431-019-0431-4

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A feline orthologue of the human MYH7 c.5647G>A (p.(Glu1883Lys)) variant causes hypertrophic cardiomyopathy in a Domestic Shorthair catPMID 31164718Read ↗

Classification of feline hypertrophic cardiomyopathy-associated gene variants according to the American College of Medical Genetics and Genomics guidelinesSemantic proximity Read ↗

Genetics of feline hypertrophic cardiomyopathy.Semantic proximity Read ↗

Identification of novel genetic variants associated with feline cardiomyopathy using targeted next-generation sequencingSemantic proximity Read ↗

The TNNT2:c.95-108G>A variant is common in Maine Coons and shows no association with hypertrophic cardiomyopathy.Semantic proximity Read ↗

A novel homozygous premature stop mutation in TNNT2 associates with Feline cardiomyopathySemantic proximity Read ↗

Identification of novel genetic variants associated with feline cardiomyopathy using targeted next-generation sequencingSemantic proximity Read ↗

Absence of known feline MYH7 and MYBPC3 variants in a diverse cohort of cats with hypertrophic cardiomyopathy.Semantic proximity Read ↗

Unraveling the genetics of feline hypertrophic cardiomyopathy: a multiomics study of 138 cats.Semantic proximity Read ↗

Genetic Basis of Hypertrophic Cardiomyopathy in CatsSemantic proximity Read ↗

Presence of known feline ALMS1 and MYBPC3 variants in a diverse cohort of cats with hypertrophic cardiomyopathy in Japan.Semantic proximity Read ↗

MYH7 in cardiomyopathy and skeletal muscle myopathy.Semantic proximity Read ↗

Myosin-binding protein C DNA variants in domestic cats (A31P, A74T, R820W) and their association with hypertrophic cardiomyopathy.Semantic proximity Read ↗

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