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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...

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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

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