Author: Weterman Marian A. J.
Publisher: Oxford University Press
ISSN: 1460-2156
Source: Brain, Vol.136, Iss.1, 2013-01, pp. : 282-293
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
Recessive twinkle mutations cause severe epileptic encephalopathy
Brain, Vol. 132, Iss. 6, 2009-06 ,pp. :
Human disease caused by loss of fast IIa myosin heavy chain due to recessive MYH2 mutations
Brain, Vol. 133, Iss. 5, 2010-05 ,pp. :
SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis
Brain, Vol. 133, Iss. 2, 2010-02 ,pp. :