Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism

CONTEXT: Necdin activates GNRH gene expression and is fundamental for the development, migration, and axonal extension of murine GNRH neurons. In humans, necdin plays a potential role in the hypogonadotropic hypogonadism phenotype in patients with Prader–Willi syndrome. AIM: To investigate necdin ge...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Beneduzzi, Daiane, Iyer, Anita K, Trarbach, Ericka Barbosa, Silveira-Neto, Acacio P, Silveira, Letícia G, Tusset, Cintia, Yip, Kathleen, Mendonça, Berenice B, Mellon, Pamela L, Latronico, Ana Claudia
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2011
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3203643/
https://ncbi.nlm.nih.gov/pubmed/21543378
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EJE-11-0199
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