Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleRecessive mutations in RYR1 are a common cause of congenital fiber type disproportion.AuthorsClarke, Nigel F.; Waddell, Leigh B.; Cooper, Sandra T.; Perry, Margaret; Smith, Robert L.L.; Kornberg, Andrew J.; Muntoni, Francesco; Lillis, Suzanne; Straub, Volker; Bushby, Kate; Guglieri, Michela; King, Mary D.; Farrell, Michael A.; Marty, Isabelle; Lunardi, Joel; Monnier, Nicole; North, Kathryn N.PublicationHuman Mutation, 2010, Vol 31, Issue 7, pE1544ISSN1059-7794Publication typeArticleDOI10.1002/humu.21278