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PubMed:18490429 / 386-523 JSONTXT 12 Projects

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Id Subject Object Predicate Lexical cue
TextSentencer_T4 0-137 Sentence denotes Mutations in human POMT1 and POMT2 cause a group of congenital muscular dystrophies due to reduced O-glycosylation of alpha-dystroglycan.
T4 0-137 Sentence denotes Mutations in human POMT1 and POMT2 cause a group of congenital muscular dystrophies due to reduced O-glycosylation of alpha-dystroglycan.
T4 0-137 Sentence denotes Mutations in human POMT1 and POMT2 cause a group of congenital muscular dystrophies due to reduced O-glycosylation of alpha-dystroglycan.