Matches in Nanopublications for { ?s ?p "[Here we describe a patient with limb girdle muscular dystrophy 1A (LGMD1A) due to a novel myotilin gene (MYOT) mutation with late onset, rapid progression, loss of ambulation and respiratory failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP804446.RAAoarxLpjalDM_ueL7L4wN2URSvu3sshV6mdpwrx5mso130_assertion description "[Here we describe a patient with limb girdle muscular dystrophy 1A (LGMD1A) due to a novel myotilin gene (MYOT) mutation with late onset, rapid progression, loss of ambulation and respiratory failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804446.RAAoarxLpjalDM_ueL7L4wN2URSvu3sshV6mdpwrx5mso130_provenance.
- NP470616.RAqBPrwNzLcHsT5txuemLvsJ4Q_hX2z1WD9remJyRmcNA130_assertion description "[Here we describe a patient with limb girdle muscular dystrophy 1A (LGMD1A) due to a novel myotilin gene (MYOT) mutation with late onset, rapid progression, loss of ambulation and respiratory failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470616.RAqBPrwNzLcHsT5txuemLvsJ4Q_hX2z1WD9remJyRmcNA130_provenance.
- NP873863.RAxb7c3ld0dQKb5Ipd-3st1nIORkzWJxMjROyVv9xMRE0130_assertion description "[Here we describe a patient with limb girdle muscular dystrophy 1A (LGMD1A) due to a novel myotilin gene (MYOT) mutation with late onset, rapid progression, loss of ambulation and respiratory failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873863.RAxb7c3ld0dQKb5Ipd-3st1nIORkzWJxMjROyVv9xMRE0130_provenance.
- assertion description "[Here we describe a patient with limb girdle muscular dystrophy 1A (LGMD1A) due to a novel myotilin gene (MYOT) mutation with late onset, rapid progression, loss of ambulation and respiratory failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP824754.RArID63kYQh-pv2uYVQeqGxd5NNOwJeeSKZoVIsehQ1NY130_assertion description "[Here we describe a patient with limb girdle muscular dystrophy 1A (LGMD1A) due to a novel myotilin gene (MYOT) mutation with late onset, rapid progression, loss of ambulation and respiratory failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824754.RArID63kYQh-pv2uYVQeqGxd5NNOwJeeSKZoVIsehQ1NY130_provenance.