Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene-disease associations and unanticipated rare disorders

Author(s):
Warrenburg, B.P.V. de; Schouten, M.I.; Bot, S.T. de; Vermeer, S.; Meijer, R.; Pennings, M.; Gilissen, C.; Willemsen, M.A.A.P.; Scheffer, H.; Kamsteeg, E.J.
Published
2016
Publication type
Article / Letter to editor
Date issued
2016-10-31
Language
English
Is part of
European Journal of Human Genetics (2016), Vol. 24, no. 10, p. 1460-1466
hdl
1887/112643
doi
10.1038/ejhg.2016.42