Matches in Nanopublications for { ?s ?p "[A novel mutation in the TTID gene results in the clinical and pathologic phenotype termed `spheroid body myopathy.` Mutations in this gene also cause limb-girdle muscular dystrophy 1A and are associated with myofibrillar myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP369004.RADl8ZGdJcu4M0PlTgEqsAbAYwN6SM7orqf11Ozr3oQFo130_assertion description "[A novel mutation in the TTID gene results in the clinical and pathologic phenotype termed `spheroid body myopathy.` Mutations in this gene also cause limb-girdle muscular dystrophy 1A and are associated with myofibrillar myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP369004.RADl8ZGdJcu4M0PlTgEqsAbAYwN6SM7orqf11Ozr3oQFo130_provenance.
- NP307305.RAPLoOb5y_--lf9XDbvr1rOLipYZ8yDFiAmRiufbbcfWo130_assertion description "[A novel mutation in the TTID gene results in the clinical and pathologic phenotype termed `spheroid body myopathy.` Mutations in this gene also cause limb-girdle muscular dystrophy 1A and are associated with myofibrillar myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307305.RAPLoOb5y_--lf9XDbvr1rOLipYZ8yDFiAmRiufbbcfWo130_provenance.