Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene
Title:
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene
Author:
Zhou, Haiyan Lillis, Suzanne Loy, Ryan E. Ghassemi, Farshid Rose, Michael R. Norwood, Fiona Mills, Kerry Al-Sarraj, Safa Lane, Russell J.M. Feng, Lucy Matthews, Emma Sewry, Caroline A. Abbs, Stephen Buk, Stefan Hanna, Michael Treves, Susan Dirksen, Robert T. Meissner, Gerhard Muntoni, Francesco Jungbluth, Heinz