Crouzon syndrome with acanthosis nigricans and prominent diffuse hyperpigmentation associated with gain-of-function A391E mutation in FGFR3 gene-论文-万方医学网

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Crouzon syndrome with acanthosis nigricans and prominent diffuse hyperpigmentation associated with gain-of-function A391E mutation in FGFR3 gene

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第一作者： Kariya, Hitomi

作者： Kariya, Hitomi ^[1] ; Nakano, Hajime ^[2] ; Ishii, Naomi ^[3] ; Kaimi, Yuto ^[4] ; Imai, Keisuke ^[5] ; Nakanishi, Yoko ; Kunihiro, Noritsugu ; Fukai, Kazuyoshi

作者单位： Osaka City Gen Hosp, Dept Dermatol, Osaka, Japan ^[1] Hirosaki Univ, Grad Sch Med, Dept Dermatol, Hirosaki, Aomori, Japan ^[2] Osaka City Gen Hosp, Dept Pathol, Osaka, Japan ^[3] Osaka City Gen Hosp, Dept Plast Surg, Osaka, Japan ^[4] Osaka City Gen Hosp, Dept Pediat Neurosurg, Osaka, Japan ^[5]

发布时间 2022-09-11

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Crouzon syndrome with acanthosis nigricans and prominent diffuse hyperpigmentation associated with gain-of-function A391E mutation in FGFR3 gene

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Crouzon syndrome with acanthosis nigricans and prominent diffuse hyperpigmentation associated with gain-of-function A391E mutation in FGFR3 gene

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同项目论文

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