伴多个扁桃体的努南综合征中同时存在 PTPN11 和 TNNT2 突变。
Mesh : Humans Protein Tyrosine Phosphatase, Non-Receptor Type 11 / genetics Noonan Syndrome / genetics Mutation Male Female Lentigo / genetics pathology N-Acetylglucosaminyltransferases / genetics
来 源: DOI:10.1093/qjmed/hcae029