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Exome sequencing revealed PMM2 gene mutations in a French-Canadian family with congenital atrophy of the cerebellum

Crossref DOI link: https://doi.org/10.1186/2053-8871-1-8

Published Online: 2014-07-04

Published Print: 2014-12

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

Authors

Noreau, Anne

Beauchemin, Philippe

Dionne-Laporte, Alexandre

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Dion, Patrick A

Rouleau, Guy A

Dupré, Nicolas
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Article History

Received: 10 April 2014

Accepted: 16 May 2014

First Online: 4 July 2014