Matches in Nanopublications for { ?s ?p "[To our knowledge, this report constitutes the first evidence of the recessive inheritance of a mutation that causes CMT2; additionally, we suggest that mutations in LMNA may also be the cause of the genetically overlapping disorder CMT2B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP3842.RAyl62z464cDOGNJae4wP6oW1r-kw15ufLE4QHOyu-ejs130_assertion description "[To our knowledge, this report constitutes the first evidence of the recessive inheritance of a mutation that causes CMT2; additionally, we suggest that mutations in LMNA may also be the cause of the genetically overlapping disorder CMT2B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3842.RAyl62z464cDOGNJae4wP6oW1r-kw15ufLE4QHOyu-ejs130_provenance.
- NP1829.RAODbhho03znjFUdn093-v0ntM3G17DFHQ_GydH2-PFeU130_assertion description "[To our knowledge, this report constitutes the first evidence of the recessive inheritance of a mutation that causes CMT2; additionally, we suggest that mutations in LMNA may also be the cause of the genetically overlapping disorder CMT2B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1829.RAODbhho03znjFUdn093-v0ntM3G17DFHQ_GydH2-PFeU130_provenance.