O6-1 Loss-of-function mutations in the gene encoding the dopamine transporter, SLC6A3, cause Infantile Parkinsonism Dystonia (IPD)

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Bibliographic Details
Published in:European journal of paediatric neurology 2009, Vol.13, p.S13-S13
Main Authors: Kurian, M.A, Zhen, J, Cheng, S.-Y, Li, Y, Mordekar, S.R, Jardine, P, Morgan, N.V, Meyer, E, Tee, L, Pasha, S, Wassmer, E, Assmann, B, Heales, S.J.R, Gissen, P, Reith, M.E.A, Maher, E.R
Format: Article
Language:English
Subjects:
Neurology
Pediatrics
Online Access:Get full text
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ISSN:1090-3798
1532-2130
DOI:10.1016/S1090-3798(09)70040-6