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Pathogenic CWF19L1 variants as a novel cause of autosomal recessive cerebellar ataxia and atrophy

Crossref DOI link: https://doi.org/10.1038/ejhg.2015.158

Published Online: 2015-07-22

Published Print: 2016-04

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Nguyen, Minh

Boesten, Iris

Hellebrekers, Debby M E I

Vanoevelen, Jo

Kamps, Rick

de Koning, Bart

de Coo, Irenaeus F M

Gerards, Mike

Smeets, Hubert J M
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Article History

Received: 26 February 2015

Revised: 9 June 2015

Accepted: 11 June 2015

First Online: 22 July 2015

Competing interests

: The authors declare no conflict of interest.