| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10745062 | Parkinsonism & Related Disorders | 2015 | 4 Pages |
Abstract
We propose that this GCH1 variant is pathogenic in this family and these findings suggest that similar mechanisms involving abnormal GTP cyclohydolase I may underlie both PD and DRD. GCH1 genetic testing should be considered in patients with PD and a family history of DRD.
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Authors
A.J. Lewthwaite, T.D. Lambert, E.B. Rolfe, S. Olgiati, M. Quadri, E.J. Simons, K.E. Morrison, V. Bonifati, D.J. Nicholl,