Matches in Nanopublications for { ?s ?p "[Mutations in the human alpha-sarcoglycan gene on chromosome 17q21.2 have been shown to cause a severe childhood autosomal recessive muscular dystrophy, a less severe limb girdle muscular dystrophy, exercise intolerance, or asymptomatic hyperCKemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP603589.RASU2WVl6Gd6W748qXcy-rJ-UCCb6vGLbhkRmQeMWI-fk130_assertion description "[Mutations in the human alpha-sarcoglycan gene on chromosome 17q21.2 have been shown to cause a severe childhood autosomal recessive muscular dystrophy, a less severe limb girdle muscular dystrophy, exercise intolerance, or asymptomatic hyperCKemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP603589.RASU2WVl6Gd6W748qXcy-rJ-UCCb6vGLbhkRmQeMWI-fk130_provenance.
- NP892194.RAwWAfOUSyfAt5eVJE2EE9Qd-erNr_aiJnRSq3SFYn9rs130_assertion description "[Mutations in the human alpha-sarcoglycan gene on chromosome 17q21.2 have been shown to cause a severe childhood autosomal recessive muscular dystrophy, a less severe limb girdle muscular dystrophy, exercise intolerance, or asymptomatic hyperCKemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892194.RAwWAfOUSyfAt5eVJE2EE9Qd-erNr_aiJnRSq3SFYn9rs130_provenance.
- assertion description "[Mutations in the human alpha-sarcoglycan gene on chromosome 17q21.2 have been shown to cause a severe childhood autosomal recessive muscular dystrophy, a less severe limb girdle muscular dystrophy, exercise intolerance, or asymptomatic hyperCKemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP418997.RAUJx_ukN5iCcHNnAk2KcWLWXIW07FN4w2ytYT4KeKBLo130_assertion description "[Mutations in the human alpha-sarcoglycan gene on chromosome 17q21.2 have been shown to cause a severe childhood autosomal recessive muscular dystrophy, a less severe limb girdle muscular dystrophy, exercise intolerance, or asymptomatic hyperCKemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418997.RAUJx_ukN5iCcHNnAk2KcWLWXIW07FN4w2ytYT4KeKBLo130_provenance.
- NP692016.RALOxNp_wnb4Ya2snzAbud43OM09qCYplPhTiJe1CXE4U130_assertion description "[Mutations in the human alpha-sarcoglycan gene on chromosome 17q21.2 have been shown to cause a severe childhood autosomal recessive muscular dystrophy, a less severe limb girdle muscular dystrophy, exercise intolerance, or asymptomatic hyperCKemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692016.RALOxNp_wnb4Ya2snzAbud43OM09qCYplPhTiJe1CXE4U130_provenance.