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Volumn 88, Issue 4, 2002, Pages 508-515
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Malignant hyperthermia associated with exercise-induced rhabdomyolysis or congenital abnormalities and a novel RYR1 mutation in New Zealand and Australian pedigrees
a b,f c c b,g a,d b b,h a e b |
Author keywords
Complications, exercise induced rhabdomyolysis; Complications, malignant hyperthermia; Complications, myopathy; Genetic factors, hyperthermia; Receptors, ryanodine
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Indexed keywords
ARGININE;
CYSTEINE;
DNA;
RYANODINE RECEPTOR;
AMINO ACID SUBSTITUTION;
ARTICLE;
AUSTRALIA;
CHROMOSOME 19Q;
CLINICAL ARTICLE;
CONTROLLED STUDY;
DISEASE ASSOCIATION;
DISEASE PREDISPOSITION;
DNA SEQUENCE;
EXERCISE;
FAMILY;
FEMALE;
GENE MUTATION;
HAPLOTYPE;
HUMAN;
HUMAN TISSUE;
IN VIVO STUDY;
MALE;
MALIGNANT HYPERTHERMIA;
MUSCLE CONTRACTURE;
MUSCULOSKELETAL SYSTEM MALFORMATION;
MYOPATHY;
NEW ZEALAND;
PEDIGREE;
PRIORITY JOURNAL;
QUADRICEPS FEMORIS MUSCLE;
RHABDOMYOLYSIS;
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EID: 18344393048
PISSN: 00070912
EISSN: None
Source Type: Journal
DOI: 10.1093/bja/88.4.508 Document Type: Article |
Times cited : (108)
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References (54)
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