Identification of a new SCN5A mutation, D1840G, associated with the long QT syndrome. Mutations in brief no. 153. Online.

Human mutation

Volumn 12, Issue 1, 1998, Pages 72-

  Benhorin, J ^a   Goldmit, M ^a   MacCluer, J W ^a   Blangero, J ^a   Goffen, R ^a   Leibovitch, A ^a   Rahat, A ^a   Wang, Q ^a   Medina, A ^a   Towbin, J ^a   Kerem, B ^a  

^a BIKUR CHOLIM HOSPITAL   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ASPARTAME; GLYCINE; SODIUM CHANNEL; VOLTAGE GATED NA+ CHANNEL NA(V)1.5A; VOLTAGE-GATED NA+ CHANNEL NA(V)1.5A;

AMINO ACID SUBSTITUTION; ARTICLE; GENETICS; HUMAN; LONG QT SYNDROME; MUTATION;

AMINO ACID SUBSTITUTION; ASPARTAME; GLYCINE; HUMANS; LONG QT SYNDROME; MUTATION; SODIUM CHANNELS;

MLCS; MLOWN;

EID: 0032222932     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1098-1004(1998)12:1<72::aid-humu17>3.0.co;2-z     Document Type: Article

References (0)