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Klippel–Trenaunay and Sturge–Weber Overlap Syndrome with KRAS and GNAQ mutations

Patients with combined phenotypes of Sturge–Weber syndrome and Klippel–Trenaunay syndrome have been reported, though the underlying genetic spectrum in these individuals remains to be elucidated. We reported the patient presenting with Klippel–Trenaunay and Sturge–Weber overlap syndrome in mainland...

詳細記述

保存先:
書誌詳細
出版年:Ann Clin Transl Neurol
主要な著者: He, Ruojie, Liao, Songjie, Yao, Xiaoli, Huang, Ruxun, Zeng, Jinsheng, Zhang, Jian, Yu, Jian
フォーマット: Artigo
言語:Inglês
出版事項: John Wiley and Sons Inc. 2020
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC7359123/
https://ncbi.nlm.nih.gov/pubmed/32613723
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.51106
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