Loss-of-Function Variants in TBC1D32 Underlie Syndromic Hypopituitarism

CONTEXT: Congenital pituitary hormone deficiencies with syndromic phenotypes and/or familial occurrence suggest genetic hypopituitarism; however, in many such patients the underlying molecular basis of the disease remains unknown. OBJECTIVE: To describe patients with syndromic hypopituitarism due to...

Descripción completa

Detalles Bibliográficos
Autores principales: Hietamäki, Johanna, Gregory, Louise C, Ayoub, Sandy, Iivonen, Anna-Pauliina, Vaaralahti, Kirsi, Liu, Xiaonan, Brandstack, Nina, Buckton, Andrew J, Laine, Tiina, Känsäkoski, Johanna, Hero, Matti, Miettinen, Päivi J, Varjosalo, Markku, Wakeling, Emma, Dattani, Mehul T, Raivio, Taneli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Clinical Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7138537/
https://www.ncbi.nlm.nih.gov/pubmed/32060556
http://dx.doi.org/10.1210/clinem/dgaa078

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7138537/
https://www.ncbi.nlm.nih.gov/pubmed/32060556
http://dx.doi.org/10.1210/clinem/dgaa078

Ejemplares similares