The Val606Met mutation of human beta myosin heavy chain in a Chinese familial hypertrophic cardiomyopathy family
Yuan, J.-s.; Qiao, S.-b.; Wang, S.-x.; Teng, S.-y.; You, S.-j.; Yang, W.-x.; Gao, R.-l.; Chen, J.-l.; Yang, Y.-j.
Zhonghua Xin Xue Guan Bing Za Zhi 36(4): 313-316
2008
ISSN/ISBN: 0253-3758 PMID: 19100006 Document Number: 617962
To explore the disease-causing gene mutation in Chinese families with hypertrophic cardiomyopathy (HCM) and to analyze the correlation between the genotype and phenotype. Samples of peripheral blood were collected from three Chinese families with HCM (at least two HCM patients existed/family). The exons in the functional regions of the beta myosin heavy chain gene (MYH7) were amplified with PCR and the products were sequenced. A Val606Met missen mutation was identified in the exon 16 of MYH7 gene in a Chinese family and this mutation was identified in all HCM patients (n = 4) and there was also a 15-years-old young mutation carrier who was not HCM patient now (penetrance of 80%). This mutation was not identified in other healthy family members in this family, in other 2 Chinese familiar HCM families and in 120 non-HCM control patients. The Val606Met missen mutation is closely associated with familiar HCM in a Chinese family which is associated with clinical phenotype with a penetrance of 80%.