Associated Papers
Whole-exome sequencing reveals MYH7 p.R671C mutation in three different phenotypes of familial hypertrophic cardiomyopathy.
Yu W et al.
Experimental and Therapeutic Medicine, 2021
[Mutation analysis of the CHD7 gene in patients with congenital heart disease].
Qi Q et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2008
[Study on mutation of presenilin-1 gene in familial Alzheimer's disease].
Liu XY et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2004
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