Author: Lönnqvist Tuula
Publisher: Oxford University Press
ISSN: 1460-2156
Source: Brain, Vol.132, Iss.6, 2009-06, pp. : 1553-1562
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
Related content
SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis
Brain, Vol. 133, Iss. 2, 2010-02 ,pp. :
Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathy
Brain, Vol. 136, Iss. 1, 2013-01 ,pp. :
A new cause of limbic encephalopathy
Brain, Vol. 128, Iss. 8, 2005-08 ,pp. :