Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course

Authors:	Luisa Sambati Raffaele Agati Antonella Bacci Silvia Bianchi Sabina Capellari

Affiliation:	1. Dipartimento di Scienze Neurologiche, IRCCS, Istituto delle Scienze Neurologiche, via Ugo Foscolo 7, Bologna, Italy 2. IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy 3. UOC di Neuroradiologia, Ospedale Bellaria, Bologna, Italy 4. Department of Neurological and Behavioral Sciences, University of Siena, Siena, Italy

Abstract:

Keywords:
本文献已被 SpringerLink 等数据库收录！