. . . . . . . "[Two patients of Charcot-Marie-Tooth disease type 1B from subsequent generations were homozygous for an Asp195Tyr mutation in the intracellular domain of P0 (P0ic).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:14:42+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .