Whole-exome sequencing identify a new mutation of MYH7 in a Chinese family with left ventricular noncompaction

Gene

Volumn 558, Issue 1, 2015, Pages 138-142

  Yang, Jing ^a,b   Zhu, Meng ^c   Wang, Yao ^a   Hou, Xiaofeng ^a   Wu, Hongping ^a   Wang, Daowu ^a   Shen, Hongbing ^c   Hu, Zhibin ^c   Zou, Jiangang ^a  

^a THE FIRST AFFILIATED HOSPITAL OF NANJING MEDICAL UNIVERSITY   (China)

^b THE AFFILIATED HUAIAN NO 1 PEOPLE S HOSPITAL OF NANJING MEDICAL UNIVERSITY   (China)

^c NANJING MEDICAL UNIVERSITY   (China)

Author keywords

Cardiomyopathy; Left ventricular noncompaction; Mutation; MYH7

Indexed keywords

DNA FRAGMENT; GENOMIC DNA; CARDIAC MYOSIN; MYH7 PROTEIN, HUMAN; MYOSIN HEAVY CHAIN;

ADULT; ARTICLE; CHINESE; ELECTROCARDIOGRAPHY; GENE; GENETIC ASSOCIATION; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MEDICAL RECORD REVIEW; MYH7 GENE; PEDIGREE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RETROSPECTIVE STUDY; SINGLE NUCLEOTIDE POLYMORPHISM; VENTRICULAR NONCOMPACTION; YOUNG ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; CONGENITAL HEART MALFORMATION; DNA SEQUENCE; EXOME; FEMALE; GENETICS; POINT MUTATION;

ASIAN CONTINENTAL ANCESTRY GROUP; CARDIAC MYOSINS; EXOME; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; MALE; MYOSIN HEAVY CHAINS; POINT MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS, DNA;

EID: 84923384877     PISSN: 03781119     EISSN: 18790038     Source Type: Journal    
DOI: 10.1016/j.gene.2014.12.061     Document Type: Article

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