Novel <i>GPC3</i> Gene Mutation in Simpson-Golabi-Behmel Syndrome with Endocrine Anomalies: A Case Report.

Bu, W; Zhu, M; Li, S; Liu, H; Liu, X

Novel GPC3 Gene Mutation in Simpson-Golabi-Behmel Syndrome with Endocrine Anomalies: A Case Report.

Bu, W; Zhu, M; Li, S; Liu, H; Liu, X.

Afiliação

Bu W; Department of Neurology, Shandong Provincial Qianfoshan Hospital, Weifang Medical University, Jinan 250014, People's Republic of China.
Zhu M; Department of Neurology, the First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan 250014, People's Republic of China.
Li S; Department of Neurology, the First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan 250014, People's Republic of China.
Liu H; Department of Neurology, Dingtao People's Hospital, Heze 274108, People's Republic of China.
Liu X; Department of Neurology, the First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan 250014, People's Republic of China.

Balkan J Med Genet ; 24(2): 95-98, 2021 Nov.

Article em En | MEDLINE | ID: mdl-36249515

Palavras-chave

Endocrine anomalies; GPC3 gene mutation; Simpson-Golabi-Behmel syndrome (SGBS)

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Balkan J Med Genet Ano de publicação: 2021 Tipo de documento: Article País de publicação: Polônia

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