Expanding the clinical phenotype associated with ELOVL4 mutation: study of a large French-Canadian family with autosomal dominant spinocerebellar ataxia and erythrokeratodermia
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| Description | article |
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author: Micheline Gravel Maxime Cadieux-Dion Anne Noreau Patrick Cossette Caroline Meloche Guy A. Rouleau |
| Publication date | April 2014 |
| Language | English |
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