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Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss

Crossref DOI link: https://doi.org/10.1007/s11033-020-05618-w

Published Online: 2020-07-04

Published Print: 2020-07

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

Authors

Sarmadi, Akram

Nasrniya, Samane

Narrei, Sina

Nouri, Zahra

Abtahi, Hamidreza

Tabatabaiefar, Mohammad Amin https://orcid.org/0000-0002-1051-3737
Funding

Funding for this research was provided by:

Isfahan University of Medical Sciences (396133, 394805, 295176)
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Article History

Received: 17 March 2020

Accepted: 22 June 2020

First Online: 4 July 2020

Compliance with ethical standards

:

: The authors declare no conflict of interest.

: The study was approved by the Review Board of Isfahan University of Medical Sciences (Grant nos. 295176, 396133 and 394805).

: Written informed consent was obtained from all of the participants in the study and a written consent to participate was obtained from the parents of the patient (younger than the age of 16). Written informed consent for publication of clinical details and clinical images was obtained from the all of the participants and from the parents the participant under the age of 18.

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