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Current Opinion in Neurology, ISSN 1350-7540, 08/2009, Volume 22, Issue 4, pp. 419 - 429
Journal Article
Book Chapter
Primary degenerative cerebellar ataxias in ethnic Bengalees in West Bengal: some observations, 12/2003
Seventy cases of primary degenerative cerebellar ataxias in ethnic Bengalees from southern West Bengal, India, were studied by the authors. Of these, 50 cases... 
Cerebellar ataxia, Autosomal recessive, Autosomal dominant, Ethnic variations
Journal
Brain, ISSN 0006-8950, 2017, Volume 140, Issue 6, pp. 1579 - 1594
Journal Article
Revue Neurologique, ISSN 0035-3787, 2011, Volume 167, Issue 5, pp. 385 - 400
Journal Article
Journal Article
Human Mutation, ISSN 1059-7794, 10/2010, Volume 31, Issue 10, pp. 1117 - 1124
Journal Article
HUMAN MUTATION, ISSN 1059-7794, 10/2010, Volume 31, Issue 10, pp. 1117 - 1124
Spinocerebellar ataxia type 28 is an autosomal dominant form of cerebellar ataxia (ADCA) caused by mutations in AFG3L2, a gene that encodes a subunit of the... 
COMPLEX | SCA28 | MITOCHONDRIA | CHAPERONE-LIKE ACTIVITY | autosomal dominant cerebellar ataxia | AFG3L2 | GENE | EXONIC SPLICING ENHANCERS | SPASTIC PARAPLEGIA | GENETICS & HEREDITY | spinocerebellar ataxia | SLOW PROGRESSION | AAA PROTEASE | Mitochondria | Missense mutation | Exons | Proteolysis |