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Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss

Crossref DOI link: https://doi.org/10.1186/1471-2164-15-1155

Published Online: 2014-12-20

Published Print: 2014-12

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

Authors

Haraksingh, Rajini R

Jahanbani, Fereshteh

Rodriguez-Paris, Juan

Gelernter, Joel

Nadeau, Kari C

Oghalai, John S

Schrijver, Iris

Snyder, Michael P
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Article History

Received: 20 March 2014

Accepted: 12 December 2014

First Online: 20 December 2014