A Balanced Translocation in Kallmann Syndrome Implicates a Long Noncoding RNA, RMST, as a GnRH Neuronal Regulator

CONTEXT: Kallmann syndrome (KS) is a rare, genetically heterogeneous Mendelian disorder. Structural defects in KS patients have helped define the genetic architecture of gonadotropin-releasing hormone (GnRH) neuronal development in this condition. OBJECTIVE: Examine the functional role a novel struc...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:J Clin Endocrinol Metab
Main Authors: Stamou, Maria, Ng, Shi-Yan, Brand, Harrison, Wang, Harold, Plummer, Lacey, Best, Lyle, Havlicek, Steven, Hibberd, Martin, Khor, Chiea Chuen, Gusella, James, Balasubramanian, Ravikumar, Talkowski, Michael, Stanton, Lawrence W, Crowley, William F
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2019
Assuntos:
Online Only
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7112981/
https://ncbi.nlm.nih.gov/pubmed/31628846
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/clinem/dgz011
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados