Produzione scientifica
Found 3 results
Filtri: Autore is Kawarai, T. [Clear All Filters]
SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis,
, Brain, Volume 133, Number 2, p.591-598, (2010)
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: A novel mutation in the SPG11 gene and further evidence for genetic heterogeneity,
, European Journal of Neurology, Volume 16, Number 1, p.121-126, (2009)
Silver syndrome variant of hereditary spastic paraplegia: A locus to 4p and allelism with SPG4,
, Neurology, Volume 70, Number 21, p.1959-1966, (2008)