HTRA1-related autosomal dominant cerebral small vessel disease

BACKGROUND: Homozygous or compound heterozygous mutations in high temperature requirement serine peptidase A1 (HTRA1) gene are responsible for cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL). Recently, increasing evidence has shown that heterozyg...

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Detalles Bibliográficos
Autores principales: Liu, Jing-Yi, Zhu, Yi-Cheng, Zhou, Li-Xin, Wei, Yan-Ping, Mao, Chen-Hui, Cui, Li-Ying, Peng, Bin, Yao, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7817319/
https://www.ncbi.nlm.nih.gov/pubmed/33109952
http://dx.doi.org/10.1097/CM9.0000000000001176

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7817319/
https://www.ncbi.nlm.nih.gov/pubmed/33109952
http://dx.doi.org/10.1097/CM9.0000000000001176

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