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Authors
Redfield, Shelby E. https://orcid.org/0000-0002-3485-6654
De-la-Torre, Pedro https://orcid.org/0000-0002-2434-3345
Zamani, Mina https://orcid.org/0000-0002-7005-3787
Wang, Hanjun
Khan, Hina
Morris, Tyler
Shariati, Gholamreza
Karimi, Majid
Kenna, Margaret A. https://orcid.org/0000-0003-0851-9272
Seo, Go Hun
Xu, Hongen
Lu, Wei
Naz, Sadaf https://orcid.org/0000-0002-1912-0235
Galehdari, Hamid
Indzhykulian, Artur A. https://orcid.org/0000-0002-2076-6818
Shearer, A. Eliot https://orcid.org/0000-0002-5324-4805
Vona, Barbara https://orcid.org/0000-0002-6719-3447
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Funding
Funding for this research was provided by:
De Garay Family Fund
Boston Children’s Rare Disease Cohort Initiative
University of the Punjab
National Institute on Deafness and Other Communication Disorders (R01DC017166)
National Institute on Deafness and Other Communication Disorders (K08 DC019716)
Deutsche Forschungsgemeinschaft (VO 2138/7-1 grant 469177153)
Herzzentrum Göttingen
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Article History
Received: 9 October 2023
Accepted: 21 January 2024
First Online: 9 March 2024
Declarations
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: Go Hun Seo is an employee of 3Billion, Inc. The other authors have no conflicts to declare.
: Written informed consent was obtained from all participants.
: Consent to publish was obtained from all participants.
: This study was approved by the institutional review boards of Boston Children’s Hospital (IRB P-00031494), University Medical Center Göttingen (No. 3/2/16), and the School of Biological Sciences, University of Punjab, Lahore, Pakistan (IRB No. 00005281).
