about
Mitochondrial dysfunction and Purkinje cell loss in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)A novel SACS gene mutation in a Tunisian family.Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family.A novel sacsin mutation in a Japanese woman showing clinical uniformity of autosomal recessive spastic ataxia of Charlevoix-Saguenay.Middle cerebellar peduncles and Pontine T2 hypointensities in ARSACS.From motor performance to participation: a quantitative descriptive study in adults with autosomal recessive spastic ataxia of Charlevoix-Saguenay
P2860
description
im Januar 2004 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в січні 2004
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name
ARSACS goes global
@en
ARSACS goes global
@nl
type
label
ARSACS goes global
@en
ARSACS goes global
@nl
prefLabel
ARSACS goes global
@en
ARSACS goes global
@nl
P356
P136
P1433
P1476
ARSACS goes global
@en
P2093
Christopher M Gomez
P356
10.1212/WNL.62.1.10
P407
P577
2004-01-13T00:00:00Z