X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene.

Kallmann syndrome represents the association of hypogonadotropic hypogonadism with anosmia. This syndrome is from a defect in the embryonic migratory pathway of gonadotropin-releasing hormone synthesizing neurons and olfactory axons. A candidate gene for the X chromosome-linked form of the syndrome...

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Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	Hardelin, J P, Levilliers, J, del Castillo, I, Cohen-Salmon, M, Legouis, R, Blanchard, S, Compain, S, Bouloux, P, Kirk, J, Moraine, C
Formato:	Artigo
Idioma:	Inglês
Publicado em:	National Academy of Sciences 1992
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC49883/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1518845/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.89.17.8190
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