. . . . . . . . . . . . "[report described the clinical features and GHR gene mutations in 2 siblings with Laron syndrome in a Chinese family; gene mutation analysis revealed that the two patients had same homozygous mutation of S65H (TCA -- > CCA) in exon 4 ]. 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 . "2014-10-02T12:33:05+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .