Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease.
Ilaria Di DonatoSilvia BianchiGian Nicola GallusAlfonso CeraseIlaria TagliaFrancesca PesciniSerena NannucciCarla BattistiDomenico InzitariLeonardo PantoniAndrea ZiniAntonio FedericoMaria Teresa DottiPublished in: CNS neuroscience & therapeutics (2017)
Our observation further supports the pathogenic role of the heterozygous HTRA1 mutations in familial SVD.