Breakpoint mapping of 13 large parkin deletions/duplications reveals an exon 4 deletion and an exon 7 duplication as founder mutations

Author(s):
Elfferich, P.; Verleun-Mooijman, M.C.; Maat-Kievit, J.A.; Warrenburg, B.P.C. van de; Abdo, W.F.; Eshuis, S.A.; Leenders, K.L.; Hovestadt, A.; Zijlmans, J.C.M.; Stroy, J.P.M.; Swieten, J.C. van; Boon, A.J.W.; Engelen, K. van; Verschuuren-Bemelmans, C.C.; Lesnik-Oberstein, S.A.J.; Tassorelli, C.; Lopiano, L.; Bonifati, V.; Dooijes, D.; Minkelen, R. van
Published
2011
Publication type
Article / Letter to editor
Parkinson's diseaseparkinDeletionDuplicationCommon founderBreakpoint mapping
Date issued
2011-11-30
Language
English
Is part of
neurogenetics (2011), Vol. 12, no. 4, p. 263-271
hdl
1887/110747
doi
10.1007/s10048-011-0302-9