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...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2011
Konular:
Article
Online Erişim: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
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller