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Parkinsonism & Related Disorders
Volume 18, Issue 2
, Pages 191-193
, February 2012
A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhood
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PII: S1353-8020(11)00323-3
doi: 10.1016/j.parkreldis.2011.10.001
© 2011 Elsevier Ltd. All rights reserved.
« Previous
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Parkinsonism & Related Disorders
Volume 18, Issue 2
, Pages 191-193
, February 2012
