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Letter to the Editor

SLC12A2: a new gene associated with autosomal dominant Non-Syndromic hearing loss in humans

ORCID Icon, , , ORCID Icon &
Pages 149-151 | Published online: 19 Feb 2020
 

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

The study has been funded by BENEFICENTIA Stiftung, which is a Foundation under Liechtenstein law having a charitable status.

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