Screening of MYH7 gene mutation sites in hypertrophic cardiomyopathy and its significance.

CONCLUSIONS: Our results showed fatal HCM harbored mutations of Thr446Pro and Phe468Leu in the MYH7 gene. It is significant for clinical and forensic medicine to further explore the functions and detailed mechanisms of these mutations.
PMID: 31503054 [PubMed - as supplied by publisher]

Source: Chinese Medical Journal - September 8, 2019 Category: General Medicine Authors: Liu HT, Ji FF, Wei L, Zuo AJ, Gao YX, Qi L, Jin B, Wang JG, Zhao P Tags: Chin Med J (Engl) Source Type: research