. . . . . . . "[However, mutations in MTM1 have also been recognized as the underlying cause of 'atypical' forms of XLMTM in newborn boys, female infants, female manifesting carriers and adult men.]. 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 . "2017-10-17T13:14:48+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .