Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients

Title
Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients
Authors
Keywords
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Journal
NEUROGENETICS
Volume 12, Issue 3, Pages 193-201
Publisher
Springer Nature
Online
2011-04-04
DOI
10.1007/s10048-011-0281-x

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