Erratum: A novel mutation of the LMNA gene in a family with dilated cardiomyopathy, conduction system disease, and sudden cardiac death of young females (Molecular and Cellular Biochemistry DOI: 10.1007/s11010-013-1734-3);A novel mutation of the LMNA gene in a family with dilated cardiomyopathy, conduction system disease, and sudden cardiac death of young females

Molecular and Cellular Biochemistry

Volumn 382, Issue 1-2, 2013, Pages 307-311

  Chen, Wenting ^a,b   Huo, Jianhua ^a   Ma, Aiqun ^a   Bai, Ling ^a   Liu, Ping ^a  

^a XI'AN JIAOTONG UNIVERSITY   (China)

^b SUZHOU MUNICIPAL HOSPITAL   (China)

Author keywords

Family dilated cardiomyopathy; Genetics; LMNA; Mutation

Indexed keywords

AMINO ACID; LAMIN A; LAMIN C; NUCLEOTIDE;

ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONGESTIVE CARDIOMYOPATHY; DISEASE SEVERITY; EXON; FEMALE; FRAMESHIFT MUTATION; GENE; GENE INSERTION; GENE MUTATION; GENETIC SCREENING; HEART FAILURE; HEART MUSCLE CONDUCTION DISTURBANCE; HUMAN; INCIDENCE; LMNA GENE; MALE; NUCLEOTIDE SEQUENCE; PHENOTYPE; PROGNOSIS; SUDDEN CARDIAC DEATH; SYMPTOMATOLOGY;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; ARRHYTHMIAS, CARDIAC; BASE SEQUENCE; CARDIOMYOPATHY, DILATED; CHILD; DEATH, SUDDEN, CARDIAC; FAMILY; FEMALE; FRAMESHIFT MUTATION; HEART CONDUCTION SYSTEM; HETEROZYGOTE; HUMANS; LAMIN TYPE A; MALE; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; YOUNG ADULT;

EID: 84884672186     PISSN: 03008177     EISSN: 15734919     Source Type: Journal    
DOI: 10.1007/s11010-013-1748-x     Document Type: Erratum

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