Abstract
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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CITATION STYLE
APA
Hara, K., Shiga, A., Fukutake, T., Nozaki, H., Miyashita, A., Yokoseki, A., … Onodera, O. (2009). Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease. New England Journal of Medicine, 360(17), 1729–1739. https://doi.org/10.1056/nejmoa0801560
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