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Neurology|January 28, 2012
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsyP Striano, Y G Weber, M R Toliat, et al.
Neurology|August 23, 2006
Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutationsH Azzedine, N Ravisé, C Verny, et al.
Neurology|May 20, 2009
SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophyM C Hannibal, E K Ruzzo, L R Miller, et al.
Neurology|September 13, 2006
Late-onset metachromatic leukodystrophy: genotype strongly influences phenotypeH Rauschka, B Colsch, N Baumann, et al.
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