The Origins of Hypertrophic Cardiomyopathy–Causing Mutations in Two South African Subpopulations: A Unique Profile of Both Independent and Founder Events
- 1 November 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 65 (5) , 1308-1320
- https://doi.org/10.1086/302623
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Identification of a new missense mutation in MyBP-C associated with hypertrophic cardiomyopathy.Journal of Medical Genetics, 1998
- Evidence of a long QT founder gene with varying phenotypic expression in South African families.Journal of Medical Genetics, 1996
- A Molecular Map of the Interactions between Titin and Myosin‐Binding Protein CEuropean Journal of Biochemistry, 1996
- Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac beta myosin heavy chain gene mutations.Heart, 1995
- The electrocardiogram is a more sensitive indicator than echocardiography of hypertrophic cardiomyopathy in families with a mutation in the MYH7 gene.Heart, 1994
- A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathyHuman Molecular Genetics, 1994
- Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene.Journal of Clinical Investigation, 1993
- Identification of a new missense mutation at Arg403, a CpG mutation hotspot, in exon 13 of the β-myosin heavy chain gene in hypertrophic cardiomyopathyHuman Molecular Genetics, 1993
- A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3Nature Genetics, 1993
- ASYMMETRICAL HYPERTROPHY OF THE HEART IN YOUNG ADULTSHeart, 1958