ATP1A3 mutations and genotype-phenotype correlation of alternating hemiplegia of childhood in chinese patients

PLoS ONE

Volumn 9, Issue 5, 2014, Pages

  Yang, Xiaoling ^a   Gao, Hua ^b   Zhang, Jie ^c   Xu, Xiaojing ^a   Liu, Xiaoyan ^a   Wu, Xiru ^a   Wei, Liping ^b,c   Zhang, Yuehua ^a  

^a PEKING UNIVERSITY FIRST HOSPITAL   (China)

^b PEKING UNIVERSITY   (China)

^c NATIONAL INSTITUTE OF BIOLOGICAL SCIENCES   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ACCURACY; ALTERNATING HEMIPLEGIA OF CHILDHOOD; ARTICLE; ATP1A3 GENE; CHILD; CHINESE; CLINICAL ARTICLE; COHORT ANALYSIS; CONTROLLED STUDY; DISEASE ASSOCIATION; EPILEPSY; EXOME; FEMALE; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENOTYPE PHENOTYPE CORRELATION; HUMAN; MALE; MISSENSE MUTATION; NEUROLOGIC DISEASE; NUCLEOTIDE SEQUENCE; ONSET AGE; POLYMERASE CHAIN REACTION; PROTEIN STRUCTURE; ADOLESCENT; ASIAN CONTINENTAL ANCESTRY GROUP; GENETIC ASSOCIATION; GENETICS; HEMIPLEGIA; INFANT; MUTATION; PRESCHOOL CHILD; PROCEDURES;

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); ATP1A3 PROTEIN, HUMAN;

ADOLESCENT; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHILD, PRESCHOOL; FEMALE; GENETIC ASSOCIATION STUDIES; HEMIPLEGIA; HUMANS; INFANT; MALE; MUTATION; SODIUM-POTASSIUM-EXCHANGING ATPASE;

EID: 84901366485     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0097274     Document Type: Article

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