Novel FGFR1 Variants Are Associated with Congenital Scoliosis

FGFR1 encodes a transmembrane cytokine receptor, which is involved in the early development of the human embryo and plays an important role in gastrulation, organ specification and patterning of various tissues. Pathogenic FGFR1 variants have been associated with Kallmann syndrome and hypogonadotrop...

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Detalles Bibliográficos
Autores principales: Wang, Shengru, Chai, Xiran, Yan, Zihui, Zhao, Sen, Yang, Yang, Li, Xiaoxin, Niu, Yuchen, Lin, Guanfeng, Su, Zhe, Wu, Zhihong, Zhang, Terry Jianguo, Wu, Nan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8393897/
https://www.ncbi.nlm.nih.gov/pubmed/34440300
http://dx.doi.org/10.3390/genes12081126

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8393897/
https://www.ncbi.nlm.nih.gov/pubmed/34440300
http://dx.doi.org/10.3390/genes12081126

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