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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease NEJM 360:1729-1739, Hara,K.,et al, 2009 See this aricle in Pubmed Article Abstract CARASIL is associated with mutations in the HTRA1 gene. Our findings indicate a link between repressed inhibition of signaling by the TGF-? family and ischemic cerebral small-vessel disease, alopecia, and spondylosis.

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