Matches in Nanopublications for { ?s ?p "[Clinical phenotype in X-linked Charcot-Marie-Tooth disease with an entire deletion of the connexin 32 coding sequence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_assertion description "[Clinical phenotype in X-linked Charcot-Marie-Tooth disease with an entire deletion of the connexin 32 coding sequence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_provenance.