Convergent biological pathways underlying the Kallmann syndrome-linked genes Hs6st1 and Fgfr1

Kallmann syndrome (KS) is a congenital disorder characterized by idiopathic hypogonadotropic hypogonadism and olfactory dysfunction. KS is linked to variants in >34 genes, which are scattered across the human genome and show disparate biological functions. Although the genetic basis of KS is well...

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Detalles Bibliográficos
Autores principales: Moon, Sohyun, Zhao, Ying-Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9759331/
https://www.ncbi.nlm.nih.gov/pubmed/35899427
http://dx.doi.org/10.1093/hmg/ddac172

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9759331/
https://www.ncbi.nlm.nih.gov/pubmed/35899427
http://dx.doi.org/10.1093/hmg/ddac172

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