A point mutation in domain 4-segment 6 of the skeletal muscle sodium channel produces an atypical inactivation state

Biophysical Journal

Volumn 78, Issue 2, 2000, Pages 773-784

  O'Reilly, John P ^a   Wang, Sho Ya ^b   Wang, Ging Kuo ^a  

^a BRIGHAM AND WOMEN S HOSPITAL   (United States)

^b STATE UNIVERSITY OF NEW YORK   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; ARGININE; ASPARTIC ACID; LYSINE; SODIUM; SODIUM CHANNEL; TYROSINE;

AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; CONFORMATIONAL TRANSITION; CONTROLLED STUDY; DEPOLARIZATION; EMBRYO; HUMAN; HUMAN CELL; NONHUMAN; PHENOTYPE; POINT MUTATION; PROTEIN DOMAIN; RAT; SKELETAL MUSCLE;

ANIMALIA;

EID: 0034128858     PISSN: 00063495     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-3495(00)76635-5     Document Type: Article

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