. . . . . . . "[Most common mutation was A922G in exon 8/exon 4 a mutation encoded C-SH2 domain of PTPN11 gene in two patients/218C-- > T mutation was found in exon 3 in a patient with Noonan syndrome and mild juvenile myelomonocytic leukaemia.]. 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 . "2017-10-17T13:15:50+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .