Novel missense mutation in cardiac troponin T gene found in Japanese patient with hypertrophic cardiomyopathy

Journal of Molecular and Cellular Cardiology

Volumn 29, Issue 2, 1997, Pages 839-843

  Nakajima Taniguchi, Chieko ^a   Matsui, Hideo ^a   Fujio, Yasushi ^a   Nagata, Seiki ^b   Kishimoto, Tadamitsu ^a   Yamauchi Takihara, Keiko ^a  

^a OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

^b KANSAI ROSAI HOSPITAL   (Japan)

Author keywords

Cardiac troponin T gene; Familial hypertrophic cardiomyopathy; Missense mutation; Phenotypic analysis

Indexed keywords

ALANINE; BINDING PROTEIN; MYOSIN HEAVY CHAIN; TROPOMYOSIN; TROPONIN T; VALINE;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CAUCASIAN; CONTROLLED STUDY; DEATH; EXON; FAMILY; FEMALE; GENE MUTATION; GENETIC HETEROGENEITY; HEART LEFT VENTRICLE HYPERTROPHY; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; JAPAN; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

GALLUS GALLUS;

EID: 0031080070     PISSN: 00222828     EISSN: None     Source Type: Journal    
DOI: 10.1006/jmcc.1996.0322     Document Type: Article

References (18)

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