Autosomal recessive spastic ataxia of Charlevoix–Saguenay

Author:

Bouchard Jean-Pierre,Richter Andrea,Mathieu Jean,Brunet Denis,Hudson Thomas J,Morgan Kenneth,Melançon Serge B

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference29 articles.

1. Eadie JM. Hereditary spastic ataxia. In: de Jong, JMBV, editor. Hereditary neuropathies and spinocerebellar atrophies. Handbook of clinical neurology, Vol. 16. Amsterdam: Elsevier, 1991:461–466.

2. Bell J, Carmichael EA. On hereditary ataxia and spastic paraplegia. In: Fisher RA, editor. Treasury of human inheritance, Vol. IV. Nervous diseases and muscular dystrophies. London: Cambridge, 1939:141–281.

3. Harding AE. Complicated forms of hereditary spastic paraplegia. The Hereditary Ataxias and Related Disorders. New York: Churchill Livingstone, 1984:191–204.

4. The Troyer syndrome. A recessive form of spastic paraplegia with distal muscle wasting;Cross;Arch Neurol (Chicago),1967

5. New type of spinocerebellar degeneration syndrome in a northern Swedish population;Gustavson;Clin Genet,1987

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