Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 2 (of 2 Records) |
Query Trace: Gingival Fibromatosis, 4[original query] |
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Screening for germline KCNQ1 and KCNE2 mutations in a set of somatotropinoma patients. Endocrine connections 2018 4 7 (5): 645-652. Iivonen Anna-Pauliina, Känsäkoski Johanna, Karppinen Atte, Kivipelto Leena, Schalin-Jäntti Camilla, Karhu Auli, Raivio Tane |
Double heterozygous pathogenic mutations in KIF3C and ZNF513 cause hereditary gingival fibromatosis. International journal of oral science 2023 9 15 (1): 46. Jianfan Chen, Xueqing Xu, Song Chen, Ting Lu, Yingchun Zheng, Zhongzhi Gan, Zongrui Shen, Shunfei Ma, Duocai Wang, Leyi Su, Fei He, Xuan Shang, Huiyong Xu, Dong Chen, Leitao Zhang, Fu Xio |
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