No missense mutation of WKL1 in a subgroup of probands with schizophrenia

Molecular Psychiatry

Volumn 7, Issue 4, 2002, Pages 419-423

  Devaney, J M ^a   Donarum, E A ^a   Brown, K M ^a   Meyer, J ^b   Stober G ^b   Lesch, K P ^b   Nestadt, G ^c   Stephan, D A ^a   Pulver, A E ^c  

^a CHILDREN'S NATIONAL MEDICAL CENTER   (United States)

^b UNIVERSITY OF WÜRZBURG   (Germany)

^c JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

22q13.33; Catatonia; Mutations; Schizophrenia; WKL1

Indexed keywords

MEMBRANE PROTEIN;

ADOLESCENT; ADULT; ALLELE; ARTICLE; CATATONIA; CHROMOSOME 22Q; CLINICAL ARTICLE; DISEASE COURSE; FEMALE; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; GERMANY; HUMAN; HUMAN CELL; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; SCHIZOPHRENIA; SCHOOL CHILD; SEGREGATION ANALYSIS; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; ADULT; CHILD; FAMILY HEALTH; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; ION CHANNELS; MALE; MUTATION, MISSENSE; SCHIZOPHRENIA, CATATONIC; UNITED STATES;

EID: 85047695612     PISSN: 13594184     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.mp.4001022     Document Type: Article

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