Detection of G338R FGFR2 mutation in a Vietnamese patient with Crouzon syndrome

Crouzon syndrome is a rare autosomal dominant genetic disorder, which causes the premature fusion of the cranial suture. Fibroblast growth factor receptor 2 (FGFR2) mutations are well-known causatives of Crouzon syndrome. The current study aimed to assess the FGFR2 gene associated with Crouzon syndr...

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Detalles Bibliográficos
Autores principales: Luong, Anh Lan Thi, Ho, Thuong Thi, Hoang, Ha, Nguyen, Trung Quang, Ho, Tu Cam, Tran, Phan Duc, Hoang, Thuy Thi, Nguyen, Nam Trung, Chu, Hoang Ha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350211/
https://www.ncbi.nlm.nih.gov/pubmed/30719288
http://dx.doi.org/10.3892/br.2019.1181

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350211/
https://www.ncbi.nlm.nih.gov/pubmed/30719288
http://dx.doi.org/10.3892/br.2019.1181

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