A carregar...

A Microdeletion of Chromosome 9q33.3 Encompasses the Entire LMX1B Gene in a Chinese Family with Nail Patella Syndrome

Nail patella syndrome (NPS) is an autosomal dominant disorder characterized by nail malformations, patellar apoplasia, or patellar hypoplasia. Mutations within the LMX1B gene are found in 85% of families with NPS; thus, this gene has been characterized as the causative gene of NPS. In this study, we...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Int J Mol Sci
Main Authors: Jiang, Shujuan, Zhang, Jiubin, Huang, Dan, Zhang, Yuanyuan, Liu, Xiaoliang, Wang, Yinzhao, He, Rong, Zhao, Yanyan
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4264161/
https://ncbi.nlm.nih.gov/pubmed/25380522
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms151120158
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!