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

CONCLUSION: Our observation further supports the pathogenic role of the heterozygous HTRA1 mutations in familial SVD. PMID: 28782182 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/28782182?dopt=Abstract

Source: CNS Neuroscience and Therapeutics - August 6, 2017 Category: Neuroscience Authors: Di Donato I, Bianchi S, Gallus GN, Cerase A, Taglia I, Pescini F, Nannucci S, Battisti C, Inzitari D, Pantoni L, Zini A, Federico A, Dotti MT Tags: CNS Neurosci Ther Source Type: research