Type 1 ryanodine receptor knock-in mutation causing central core disease of skeletal muscle also displays a neuronal phenotype

Proceedings of the National Academy of Sciences of the United States of America

Volumn 109, Issue 2, 2012, Pages 610-615

  De Crescenzo, Valerie ^a   Fogarty, Kevin E ^a   Lefkowitz, Jason J ^a   Bellve, Karl D ^a   Zvaritch, Elena ^b   MacLennan, David H ^b   Walsh, John V ^a  

^a UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF TORONTO   (Canada)

Author keywords

Exocytosis; Microdomain; Oxytocin vasopressin

Indexed keywords

RYANODINE RECEPTOR 1; VOLTAGE GATED CALCIUM CHANNEL;

ANIMAL EXPERIMENT; ARTICLE; CALCIUM TRANSPORT; CENTRAL CORE DISEASE; CONTROLLED STUDY; DEPOLARIZATION; EXTRACELLULAR CALCIUM; GENE MUTATION; GENE REPLICATION; GENE TARGETING; MOUSE; NERVE ENDING; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; SKELETAL MUSCLE;

MUS;

EID: 84855989743     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1115111108     Document Type: Article

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