Autosomal dominant cerebral small vessel disease associated with HTRA1 gene mutation in an Italian family

Autor: Veneziano L (1), Mantuano E (1), Romano S (2), Spadaro M (1), Amadoro G (1), Frontali M (1)

Publikováno v: European Human Genetics Conference 2016, pp. 446–446, Barcellona, Spain, 21-24/5/2016
info:cnr-pdr/source/autori:Veneziano L (1), Mantuano E (1), Romano S (2), Spadaro M (1), Amadoro G (1), Frontali M (1)/congresso_nome:European Human Genetics Conference 2016/congresso_luogo:Barcellona, Spain/congresso_data:21-24%2F5%2F2016/anno:2016/pagina_da:446/pagina_a:446/intervallo_pagine:446–446

Introduction: Cerebral small vessel diseases (CSVDs) are an important cause of stroke, cognitive impairment, and mood disorders among the elderly. Usually CSVD is sporadic, but early-onset monogenic forms of CSVD have been reported. CADASIL is one of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::42c0eee5625976638968ed924a2ad027
http://www.cnr.it/prodotto/i/370370