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Atypical Friedreich ataxia in patients with FXN p.R165P point mutation or comorbid hemochromatosis

✍ Scribed by Ygland, Emil; Taroni, Franco; Gellera, Cinzia; Caldarazzo, Serena; Duno, Morten; Soller, Maria; Puschmann, Andreas


Book ID
122118653
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
454 KB
Volume
20
Category
Article
ISSN
1353-8020

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