No NRG1 V266L in Chinese patients with schizophrenia

Psychiatric Genetics

Volumn 21, Issue 1, 2011, Pages 47-49

  Garcia Barceló, Maria Mercè ^a   Miao, Xiaoping ^a,e   Tang, Clara S ^a   So, Hon Cheong ^a   Tang, Waikiu ^a   Leon, Thomas Y Y ^a   So, Manting ^a   Yip, Benjamin ^a   Chen, Ronald Y L ^a   Cheung, Eric F C ^c   Chen, Eric Y H ^d   Li, Tao ^d,f   Tam, Paul ^a   Cherny, Stacey S ^a,b   Sham, Pak C ^a,b  

^a UNIVERSITY OF HONG KONG   (Hong Kong)

^b UNIVERSITY OF HONG KONG   (Hong Kong)

^c CASTLE PEAK HOSPITAL   (Hong Kong)

^d SICHUAN UNIVERSITY   (China)

^e HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^f KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

mutations; neuregulin 1; V266L

Indexed keywords

ARTICLE; CHINESE; CONTROLLED STUDY; GENE; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; HUMAN; MAJOR CLINICAL STUDY; MISSENSE MUTATION; NRG1 GENE; PRIORITY JOURNAL; SCHIZOPHRENIA;

AMINO ACID SUBSTITUTION; ASIAN CONTINENTAL ANCESTRY GROUP; CHINA; GENE FREQUENCY; HUMANS; LINKAGE DISEQUILIBRIUM; NEUREGULIN-1; POLYMORPHISM, SINGLE NUCLEOTIDE; REPRODUCIBILITY OF RESULTS; SCHIZOPHRENIA;

EID: 78650772199     PISSN: 09558829     EISSN: None     Source Type: Journal    
DOI: 10.1097/YPG.0b013e328341355b     Document Type: Article

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