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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
Author(s) -
Kenju Hara,
Atsushi Shiga,
Toshio Fukutake,
Hiroaki Nozaki,
Akinori Miyashita,
Akio Yokoseki,
Hirotoshi Kawata,
Akihide Koyama,
Kunimasa Arima,
Toshiaki Takahashi,
Mari Ikeda,
Hiroshi Shiota,
Masato Tamura,
Yutaka Shimoe,
Masaaki Hirayama,
Takayo Arisato,
S Yanagawa,
Akira Tanaka,
Imaharu Nakano,
Shuichi Ikeda,
Yutaka Yoshida,
Tadashi Yamamoto,
Takeshi Ikeuchi,
Ryozo Kuwano,
Masatoyo Nishizawa,
Shoji Tsuji,
Osamu Onodera
Publication year - 2009
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa0801560
Subject(s) - medicine , disease , association (psychology) , cardiology , epistemology , philosophy
The genetic cause of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL), which is characterized by ischemic, nonhypertensive, cerebral small-vessel disease with associated alopecia and spondylosis, is unclear.

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