Molecular Basis for Autosomal-Dominant Renal Fanconi Syndrome Caused by HNF4A

HNF4A is a nuclear hormone receptor that binds DNA as an obligate homodimer. While all known human heterozygous mutations are associated with the autosomal-dominant diabetes form MODY1, one particular mutation (p.R85W) in the DNA-binding domain (DBD) causes additional renal Fanconi syndrome (FRTS)....

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Cell Rep
Main Authors: Marchesin, Valentina, Pérez-Martí, Albert, Le Meur, Gwenn, Pichler, Roman, Grand, Kelli, Klootwijk, Enriko D., Kesselheim, Anne, Kleta, Robert, Lienkamp, Soeren, Simons, Matias
Formato: Artigo
Idioma:Inglês
Publicado em: Cell Press 2019
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6941224/
https://ncbi.nlm.nih.gov/pubmed/31875549
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.celrep.2019.11.066
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados