Matches in Nanopublications for { ?s ?p "[The severe neonatal X-linked form (myotubular myopathy) is due to mutations in the phosphoinositide phosphatase myotubularin (MTM1), whereas mutations in dynamin 2 (DNM2) have been found in some autosomal dominant cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[The severe neonatal X-linked form (myotubular myopathy) is due to mutations in the phosphoinositide phosphatase myotubularin (MTM1), whereas mutations in dynamin 2 (DNM2) have been found in some autosomal dominant cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The severe neonatal X-linked form (myotubular myopathy) is due to mutations in the phosphoinositide phosphatase myotubularin (MTM1), whereas mutations in dynamin 2 (DNM2) have been found in some autosomal dominant cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The severe neonatal X-linked form (myotubular myopathy) is due to mutations in the phosphoinositide phosphatase myotubularin (MTM1), whereas mutations in dynamin 2 (DNM2) have been found in some autosomal dominant cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP623587.RAi-k5ckG11XgUEMS5qDfEpAn2zeE41IsLyTe1KYLo9Lg130_assertion description "[The severe neonatal X-linked form (myotubular myopathy) is due to mutations in the phosphoinositide phosphatase myotubularin (MTM1), whereas mutations in dynamin 2 (DNM2) have been found in some autosomal dominant cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623587.RAi-k5ckG11XgUEMS5qDfEpAn2zeE41IsLyTe1KYLo9Lg130_provenance.
- NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_assertion description "[The severe neonatal X-linked form (myotubular myopathy) is due to mutations in the phosphoinositide phosphatase myotubularin (MTM1), whereas mutations in dynamin 2 (DNM2) have been found in some autosomal dominant cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_provenance.