Phenotypic variability in a dystonia family with mutations in the manganese transporter gene.
Autor: | Delnooz CC, Wevers RA, Quadri M, Clayton PT, Mills PB, Tuschl K, Steenbergen EJ, Bonifati V, van de Warrenburg BP |
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Jazyk: | angličtina |
Zdroj: | Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2013 May; Vol. 28 (5), pp. 685-6. Date of Electronic Publication: 2013 Apr 16. |
DOI: | 10.1002/mds.25390 |
Databáze: | MEDLINE |
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