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Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37

Crossref DOI link: https://doi.org/10.1038/s41436-018-0285-0

Published Print: 2019-04

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Booth, Kevin T.

Askew, James W.

Talebizadeh, Zohreh

Huygen, Patrick L.M.

Eudy, James

Kenyon, Judith

Hoover, Denise

Hildebrand, Michael S.

Smith, Katherine R.

Bahlo, Melanie

Kimberling, William J.

Smith, Richard J.H.

Azaiez, Hela

Smith, Shelley D.
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Text and Data Mining valid from 2019-04-01

Text and Data Mining valid from 2019-04-01

Version of Record valid from 2021-11-24
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This article is maintained by: Elsevier

Article Title: Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-018-0285-0

Content Type: article

Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics