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Trends in Molecular Medicine|October 17, 2012
Mapping domains and mutations on the skeletal muscle ryanodine receptor channelJean H Hwang, Francesco Zorzato, Nigel F Clarke, et al.
Orphanet Journal of Rare Diseases|August 8, 2013
Genotype-phenotype correlations in recessive RYR1-related myopathiesKimberly Amburgey, Angela Bailey, Jean H Hwang, et al.
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