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Familial Hypertrophic Cardiomyopathy Associated with Cardiac β-Myosin Heavy Chain and Troponin I Mutations

✍ Scribed by Aisha Frazier; Daniel P. Judge; Steven P. Schulman; Nicole Johnson; Kathryn W. Holmes; Anne M. Murphy


Publisher
Springer
Year
2008
Tongue
English
Weight
249 KB
Volume
29
Category
Article
ISSN
0172-0643

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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