학술논문
Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPMmutations
Document Type
Article
Author
Passemard, S; Titomanlio, L; Elmaleh, M; Afenjar, A; Alessandri, J -L.; Andria, G; Villemeur, T Billette de; Boespflug-Tanguy, O; Burglen, L; Del Giudice, E; Guimiot, F; Hyon, C; Isidor, B; Mégarbané, A; Moog, U; Odent, S; Hernandez, K; Pouvreau, N; Scala, I; Schaer, M; Gressens, P; Gerard, B; Verloes, A
Source
Neurology (Ovid); September 2009, Vol. 73 Issue: 12 p962-969, 8p
Subject
Language
ISSN
00283878; 1526632X
Abstract
To determine the spectrum of clinical, neuropsychological, and neuroradiologic features in patients with autosomal recessive primary microcephaly (MCPH) due to ASPMgene mutations.