Matches in Nanopublications for { ?s ?p "[Myotubularin (hMTM1), the founder member, is mutated in myotubular myopathy, and a close homolog (hMTMR2) was recently found mutated in a recessive form of Charcot-Marie-Tooth neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 11 of
11
with 100 items per page.
- NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_assertion description "[Myotubularin (hMTM1), the founder member, is mutated in myotubular myopathy, and a close homolog (hMTMR2) was recently found mutated in a recessive form of Charcot-Marie-Tooth neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP759466.RAmwXIF1WhFs-6cigF0fOn2dEpsahYZI2ewo1eNXAmB8k130_provenance.
- NP641035.RAdr0Q3-ugrZ8hbYI3K09X8e27eWrxShU-qFCWKLZc7kk130_assertion description "[Myotubularin (hMTM1), the founder member, is mutated in myotubular myopathy, and a close homolog (hMTMR2) was recently found mutated in a recessive form of Charcot-Marie-Tooth neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641035.RAdr0Q3-ugrZ8hbYI3K09X8e27eWrxShU-qFCWKLZc7kk130_provenance.
- assertion description "[Myotubularin (hMTM1), the founder member, is mutated in myotubular myopathy, and a close homolog (hMTMR2) was recently found mutated in a recessive form of Charcot-Marie-Tooth neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Myotubularin (hMTM1), the founder member, is mutated in myotubular myopathy, and a close homolog (hMTMR2) was recently found mutated in a recessive form of Charcot-Marie-Tooth neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Myotubularin (hMTM1), the founder member, is mutated in myotubular myopathy, and a close homolog (hMTMR2) was recently found mutated in a recessive form of Charcot-Marie-Tooth neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP576397.RADQIv922rYS6eeRZZPrp-rHYKn2_oWva8IQM9UeO6CN8130_assertion description "[Myotubularin (hMTM1), the founder member, is mutated in myotubular myopathy, and a close homolog (hMTMR2) was recently found mutated in a recessive form of Charcot-Marie-Tooth neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576397.RADQIv922rYS6eeRZZPrp-rHYKn2_oWva8IQM9UeO6CN8130_provenance.
- NP312389.RAgzQ5U2ogv6Qp7jjN8K-Q1gRituvmLFXBvX4Xnuamu1o130_assertion description "[Myotubularin (hMTM1), the founder member, is mutated in myotubular myopathy, and a close homolog (hMTMR2) was recently found mutated in a recessive form of Charcot-Marie-Tooth neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312389.RAgzQ5U2ogv6Qp7jjN8K-Q1gRituvmLFXBvX4Xnuamu1o130_provenance.
- NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_assertion description "[Myotubularin (hMTM1), the founder member, is mutated in myotubular myopathy, and a close homolog (hMTMR2) was recently found mutated in a recessive form of Charcot-Marie-Tooth neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312390.RAh8SpA2cnFfAHZ7hSrEYVUVmJpc6A1_tVo8lk2tQgqFQ130_provenance.
- NP312391.RAvaavE1WcPeA0hlGZQ4jYzQQ4C1oeThjl2MxRQ3gxtS0130_assertion description "[Myotubularin (hMTM1), the founder member, is mutated in myotubular myopathy, and a close homolog (hMTMR2) was recently found mutated in a recessive form of Charcot-Marie-Tooth neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312391.RAvaavE1WcPeA0hlGZQ4jYzQQ4C1oeThjl2MxRQ3gxtS0130_provenance.
- NP576461.RAKwUAqdv14PsgHpLNs_3qBO7shlp4kfh_ePMASLkF8BA130_assertion description "[Myotubularin (hMTM1), the founder member, is mutated in myotubular myopathy, and a close homolog (hMTMR2) was recently found mutated in a recessive form of Charcot-Marie-Tooth neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576461.RAKwUAqdv14PsgHpLNs_3qBO7shlp4kfh_ePMASLkF8BA130_provenance.
- NP312388.RA18A6I7hvaE5wQW0qyvN7fMPBd0uAwUpeOphYmMQXk44130_assertion description "[Myotubularin (hMTM1), the founder member, is mutated in myotubular myopathy, and a close homolog (hMTMR2) was recently found mutated in a recessive form of Charcot-Marie-Tooth neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312388.RA18A6I7hvaE5wQW0qyvN7fMPBd0uAwUpeOphYmMQXk44130_provenance.