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
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