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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2022
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| 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 |