A carregar...

A novel MPV17 gene mutation in a Saudi infant causing fatal progressive liver failure

We describe in this report the clinical, biochemical, and molecular features of a Saudi infant with hepatocerebral MDS secondary to a novel homozygous mutation in the MPV17 gene. An automated sequencing of the nuclear MPV17 gene was performed. The coding region (7 exons) of the MPV17 gene was amplif...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Ann Saudi Med
Main Authors: Al Sarkhy, Ahmed, Al-Sunaid, Areej, Abdullah, Ahmad, AlFadhel, Majid, Eiyad, Wafa
Formato: Artigo
Idioma:Inglês
Publicado em: King Faisal Specialist Hospital and Research Centre 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6074855/
https://ncbi.nlm.nih.gov/pubmed/24894789
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5144/0256-4947.2014.175
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!