Referenced in: none

Automatically associated channels: Cav1.1 , Kir6.2 , Nav1.4

Title: Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene.

Authors: Haiyan Zhou, Suzanne Lillis, Ryan E Loy, Farshid Ghassemi, Michael R Rose, Fiona Norwood, Kerry Mills, Safa Al-Sarraj, Russell J M Lane, Lucy Feng, Emma Matthews, Caroline A Sewry, Stephen Abbs, Stefan Buk, Michael Hanna, Susan Treves, Robert T Dirksen, Gerhard Meissner, Francesco Muntoni, Heinz Jungbluth

Journal, date & volume: Neuromuscul. Disord., 2010 Mar , 20, 166-73

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/20080402

Abstract