. . . . . . . "[Here, we report the first homozygous mutation in the PPP1R15B gene (also known as constitutive repressor of eIF2? phosphorylation [CReP]) encoding the regulatory subunit of an eIF2?-specific phosphatase in two siblings affected by a novel syndrome of diabetes of youth with short stature, intellectual disability, and microcephaly.]. 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 . "2017-10-17T13:19:00+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .