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Article

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3

1 Apr 1993

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 7981753
DOI: 10.1038/ng0493-333

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3PMID 7981753Read ↗

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Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathy.Semantic proximity Read ↗

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Mapping a cardiomyopathy locus to chromosome 3p22-p25.Semantic proximity Read ↗

Variant Spectrum of Formin Homology 2 Domain-Containing 3 Gene in Chinese Patients With Hypertrophic Cardiomyopathy.Semantic proximity Read ↗

Symposium on gene abnormalities in medical diseases. 3. Molecular genetics of hypertrophic cardiomyopathy in Japan.Semantic proximity Read ↗

Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3.Semantic proximity Read ↗

Intermediate-effect size p.Arg637Gln in FHOD3 increases risk of HCM and is associated with an aggressive phenotype in homozygous carriers.Semantic proximity Read ↗

CSRP3, p.Arg122*, is responsible for hypertrophic cardiomyopathy in a Chinese family.Semantic proximity Read ↗

A Pathogenic Variant inALPK3Is Associated With an Autosomal Dominant Adult-onset Hypertrophic CardiomyopathySemantic proximity Read ↗

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