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Deletion of AFG3L2 associated with spinocerebellar ataxia type 28 in the context of multiple genomic anomalies
Myers, Kenneth A., Warman Chardon, Jodi, Huang, Lijia, Boycott, Kym M.Volume:
164
Language:
english
Journal:
American Journal of Medical Genetics Part A
DOI:
10.1002/ajmg.a.36771
Date:
December, 2014
File:
PDF, 215 KB
english, 2014