Heterozygous HTRA1 missense mutation in CADASIL-like family disease

The aim of this study was to find related pathogenic genes in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in (CADASIL)-like patients. The direct sequencing and high-throughput multiplex polymerase chain reaction (PCR) was performed to screen for related...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Xiaowei, Li, Changxin, Mao, Jinming, Li, Ling, Liu, Yan, Hou, Yao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Divulgação Científica 2018
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5875909/
https://www.ncbi.nlm.nih.gov/pubmed/29561953
http://dx.doi.org/10.1590/1414-431X20176632

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5875909/
https://www.ncbi.nlm.nih.gov/pubmed/29561953
http://dx.doi.org/10.1590/1414-431X20176632

Ejemplares similares