Matches in Nanopublications for { ?s ?p "[The Spanish cohort, the largest group of patients studied so far, shares phenotypic features with both LGMD1A and MFM/MYOT variants thus establishing a continuum of phenotypic manifestations characteristic of myotilinopathy, an emerging neuromuscular disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_assertion description "[The Spanish cohort, the largest group of patients studied so far, shares phenotypic features with both LGMD1A and MFM/MYOT variants thus establishing a continuum of phenotypic manifestations characteristic of myotilinopathy, an emerging neuromuscular disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800036.RAquY866qcupuShS1ra4SyWWMgERudTBq-V78fWrvXboE130_provenance.
- NP856336.RAdQgIjWojoUbqb6KKysKu87T5WfwE6ycX0quL-tAsqJk130_assertion description "[The Spanish cohort, the largest group of patients studied so far, shares phenotypic features with both LGMD1A and MFM/MYOT variants thus establishing a continuum of phenotypic manifestations characteristic of myotilinopathy, an emerging neuromuscular disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856336.RAdQgIjWojoUbqb6KKysKu87T5WfwE6ycX0quL-tAsqJk130_provenance.
- assertion description "[The Spanish cohort, the largest group of patients studied so far, shares phenotypic features with both LGMD1A and MFM/MYOT variants thus establishing a continuum of phenotypic manifestations characteristic of myotilinopathy, an emerging neuromuscular disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP824757.RAptx3tOz6gCzkC4tq6BNc5KDs-uROter3nlv1VjU93zI130_assertion description "[The Spanish cohort, the largest group of patients studied so far, shares phenotypic features with both LGMD1A and MFM/MYOT variants thus establishing a continuum of phenotypic manifestations characteristic of myotilinopathy, an emerging neuromuscular disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824757.RAptx3tOz6gCzkC4tq6BNc5KDs-uROter3nlv1VjU93zI130_provenance.
- NP498684.RAiEn-zv_Rb4cbIv9CWW6MMaGdYhB0unWAAC6MwDzm8YQ130_assertion description "[The Spanish cohort, the largest group of patients studied so far, shares phenotypic features with both LGMD1A and MFM/MYOT variants thus establishing a continuum of phenotypic manifestations characteristic of myotilinopathy, an emerging neuromuscular disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP498684.RAiEn-zv_Rb4cbIv9CWW6MMaGdYhB0unWAAC6MwDzm8YQ130_provenance.