Phenotype-genotype analysis of Chinese patients with early-onset LMNA-related muscular dystrophy

PLoS ONE

Volumn 10, Issue 6, 2015, Pages

  Tan, Dandan ^a,b   Yang, Haipo ^a   Yuan, Yun ^a   Bonnemann, Carsten ^c   Chang, Xingzhi ^a   Wang, Shuang ^a   Wu, Yuchen ^b   Wu, Xiru ^a   Xiong, Hui ^a  

^a PEKING UNIVERSITY FIRST HOSPITAL   (China)

^b NANCHANG UNIVERSITY   (China)

^c NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LAMIN A; LMNA PROTEIN, HUMAN;

ARTICLE; CHILD; CHINESE; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; DNA SEQUENCE; FEMALE; GENE; GENE DELETION; GENETIC ASSOCIATION; GENETIC CONSERVATION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOREACTIVITY; INFANT; LMNA GENE; MALE; MISSENSE MUTATION; MUSCULAR DYSTROPHY; MUTATIONAL ANALYSIS; ONSET AGE; PATHOGENESIS; PROTEIN LOCALIZATION; RETROSPECTIVE STUDY; FIBROBLAST; GENETICS; GENOTYPE; METABOLISM; MUSCULAR DYSTROPHY, EMERY-DREIFUSS; PHENOTYPE; PRESCHOOL CHILD;

CHILD; CHILD, PRESCHOOL; FEMALE; FIBROBLASTS; GENOTYPE; HUMANS; INFANT; LAMIN TYPE A; MALE; MUSCULAR DYSTROPHY, EMERY-DREIFUSS; MUTATION, MISSENSE; PHENOTYPE;

EID: 84939199989     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0129699     Document Type: Article

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