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Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease

CNS Neuroscience & Therapeutics Aug 26, 2017

Di Donato I, et al. – The authors conducted a mutational analysis of HTRA1 gene in a large cohort of Italian NOTCH3–negative patients to detect a genetic cause of familial small vessel disease (SVD). This observation further bolsters the pathogenic role of the heterozygous HTRA1 mutations in familial SVD.
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