. . . . . . . "[In addition, next generation sequencing of 52 genes for hereditary neuropathies revealed a heterozygous missense mutation c.505T?>?C; p.Y169H in the SH3TC2 gene that was transmitted by the healthy father.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:18:53+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .