A missense mutation in a novel gene encoding a putative cation channel is associated with catatonic schizophrenia in a large pedigree

Molecular Psychiatry

Volumn 6, Issue 3, 2001, Pages 302-306

  Meyer, J ^a   Huberth, A ^a   Ortega, G ^a   Syagailo, Y V ^a   Jatzke, S ^a   Mossner R ^a   Strom, T M ^b   Ulzheimer Teuber, I ^a   Stober G ^a   Schmitt, A ^a   Lesch, K P ^a  

^a UNIVERSITY OF WÜRZBURG   (Germany)

^b INSTITUTE OF EPIDEMIOLOGY   (Germany)

Author keywords

22q13.33; Cation channel; Genetics; Heterogeneity; Mutation; Schizophrenia

Indexed keywords

CATION CHANNEL; MUTANT PROTEIN;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 22Q; FAMILIAL DISEASE; GENE EXPRESSION; GENE SEGREGATION; GENETIC HETEROGENEITY; HUMAN; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; PRIORITY JOURNAL; PROTEIN CONFORMATION; SCHIZOPHRENIA;

AMINO ACID SEQUENCE; BRAIN CHEMISTRY; CHROMOSOMES, HUMAN, PAIR 22; FAMILY HEALTH; FEMALE; GENETIC HETEROGENEITY; HUMANS; ION CHANNELS; MALE; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; PEDIGREE; SCHIZOPHRENIA, CATATONIC;

EID: 17744384259     PISSN: 13594184     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.mp.4000869     Document Type: Article

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