HTRA1-related autosomal dominant cerebral small vessel disease

HTRA1-related autosomal dominant cerebral small vessel disease

Abstract. 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...

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Bibliographic Details
Main Authors: Jing-Yi Liu, Yi-Cheng Zhu, Li-Xin Zhou, Yan-Ping Wei, Chen-Hui Mao, Li-Ying Cui, Bin Peng, Ming Yao, Xin Chen
Format: Article
Language:English
Published: Wolters Kluwer 2021-01-01
Series:Chinese Medical Journal
Online Access:http://journals.lww.com/10.1097/CM9.0000000000001176

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http://journals.lww.com/10.1097/CM9.0000000000001176

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