Identification of the gene for Nance-Horan syndrome (NHS)

Background: The disease intervals for Nance-Horan syndrome (NHS [MIM 302350]) and X linked congenital cataract (CXN) overlap on Xp22. Objective: To identify the gene or genes responsible for these diseases. Methods: Families with NHS were ascertained. The refined locus for CXN was used to focus the...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Brooks, S, Ebenezer, N, Poopalasundaram, S, Lehmann, O, Moore, A, Hardcastle, A
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2004
Assuntos:
Short Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735593/
https://ncbi.nlm.nih.gov/pubmed/15466011
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.022517
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados