Citations for
1ADCY5, ANO3, DTPC3, DYT5, FDFM, GCH1
Clinical exome sequencing in early-onset generalized dystonia and large-scale resequencing follow-up.
Zech M, Boesch S, Jochim A, Weber S, Meindl T, Schormair B, Wieland T, Lunetta C, Sansone V, Messner M, Mueller J, Ceballos-Baumann A, Strom TM, Colombo R, Poewe W, Haslinger B, Winkelmann J.
Mov Disord ov Disord. 2016 Sep 26. doi: 10.1002/mds.26808. [Epub ahead of print] 2016
2ADCY5, DYT10, DYT10, DYT8, FDFM, GCH1, PNKD, PRRT2
Paroxysmal movement disorders: An update.
Méneret A, Roze E.
Rev Neurol (Paris) 172(8-9):433-445. doi: 10.1016/j.neurol.2016.07.005. 2016
3FDFM
Familial dyskinesia and facial myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21.
Raskind WH, Matsushita M, Peter B, Biberston J, Wolff J, Lipe H, Burbank R, Bird TD.
Am J Med Genet B Neuropsychiatr Genet 150B(4):570-4. 2009
4FDFM
Familial dyskinesia and facial myokymia (FDFM): a novel movement disorder.
Fernandez M, Raskind W, Wolff J, Matsushita M, Yuen E, Graf W, Lipe H, Bird T.
Ann Neurol 49(4):486-92. 2001