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Exome sequencing identifies pathogenic variants of VPS13B in a patient with familial 16p11.2 duplication

Crossref DOI link: https://doi.org/10.1186/s12881-016-0340-0

Published Online: 2016-11-10

Published Print: 2016-12

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

Authors

Dastan, Jila

Chijiwa, Chieko

Tang, Flamingo

Martell, Sally

Qiao, Ying

Rajcan-Separovic, Evica

Lewis, M. E. Suzanne
Funding

Funding for this research was provided by:

Canadian Institutes for Health Research (MOP-74502)

BC Children’s Hospital Foundation (KRZ75146)

BC Child and Family Research Institute (20R20410)
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Article History

Received: 3 May 2016

Accepted: 20 October 2016

First Online: 10 November 2016