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pubmed-article:18036232pubmed:abstractTextThere is a marked variation in clinical phenotypes that have been associated with mutations in FKRP, ranging from severe congenital muscular dystrophies to limb-girdle muscular dystrophy type 2I (LGMD2I).lld:pubmed
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pubmed-article:18036232pubmed:articleTitleLGMD2I in a North American population.lld:pubmed
pubmed-article:18036232pubmed:affiliationProgram in Genomics, Children's Hospital Boston and Harvard Medical School, Boston, USA. peter.kang@childrens.harvard.edulld:pubmed
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