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A novel mutation in SACS gene in a family from southern Italy

Academic Article
Publication Date:
2004
abstract:
A form of autosomal recessive spastic ataxia (ARSACS) has been described in the Charlevoix and Saguenay regions of Quebec. So far a frameshift and a nonsense mutation have been identified in the SACS gene. The authors report a new mutation (1859insC), leading to a frameshift with a premature termination of the gene product sacsin, in two sisters from consanguineous parents. The phenotype is similar to previously described patients with ARSACS.
Iris type:
01.01 Articolo in rivista
List of contributors:
Monticelli, Antonella
Handle:
https://iris.cnr.it/handle/20.500.14243/51076
Published in:
NEUROLOGY
Journal
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