Matches in Nanopublications for { ?s ?p "[X-linked Charcot-Marie-Tooth disease (CMT1X) is a peripheral neuropathy transmitted in a dominant manner and caused by mutations in the Connexin 32 (Cx32) gene (GJB1, gap junction beta 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP366720.RAH_BreexoKK6iMyKTjh_8OWKHW0FRLFuUdKEmah_R0AQ130_assertion description "[X-linked Charcot-Marie-Tooth disease (CMT1X) is a peripheral neuropathy transmitted in a dominant manner and caused by mutations in the Connexin 32 (Cx32) gene (GJB1, gap junction beta 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP366720.RAH_BreexoKK6iMyKTjh_8OWKHW0FRLFuUdKEmah_R0AQ130_provenance.
- NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_assertion description "[X-linked Charcot-Marie-Tooth disease (CMT1X) is a peripheral neuropathy transmitted in a dominant manner and caused by mutations in the Connexin 32 (Cx32) gene (GJB1, gap junction beta 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_provenance.
- NP663248.RANLJxlAXWCwXU4J90tZ3M3jxV7ybx2_WJuHhKwATT_cA130_assertion description "[X-linked Charcot-Marie-Tooth disease (CMT1X) is a peripheral neuropathy transmitted in a dominant manner and caused by mutations in the Connexin 32 (Cx32) gene (GJB1, gap junction beta 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663248.RANLJxlAXWCwXU4J90tZ3M3jxV7ybx2_WJuHhKwATT_cA130_provenance.