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Genotype-phenotype correlation of R870H mutation in hypertrophic cardiomyopathy

✍ Scribed by RR Tanjore; AD Sikindlapuram; N Calambur; B Thakkar; PG Kerkar; P Nallari


Book ID
110888184
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
87 KB
Volume
69
Category
Article
ISSN
0009-9163

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Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease in which one of the most frequently implicated gene is the gene encoding the b-myosin heavy chain. To date, more than 40 distinct mutations have been found within this gene. In order to progress on the determination of genot