Novel Mutations in FGFR1 Causing Idiopathic Hypogonadotropic Hypogonadism: A Cohort Study in Eastern Indian Population

Introduction: IHH is a clinically and genetically heterogeneous condition with more than 80 different mutations described in literature, some of the important being KAL-1 (anosmin), fibroblast growth factor receptor-1 (FGFR1) and fibroblast growth factor-8 (FGF8). Objective: To characterize the clin...

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Detalles Bibliográficos
Autores principales: Baidya, Arjun, Datta, Saptarshi, Mukhopadhyay, Satinath, Roy, Sib Shankar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Genetics and Development (including Gene Regulation)
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8090713/
http://dx.doi.org/10.1210/jendso/bvab048.1038

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8090713/
http://dx.doi.org/10.1210/jendso/bvab048.1038

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