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Whole-exome sequencing reveals a rare missense variant in DTNA in an Iranian pedigree with early-onset atrial fibrillation

Published Online: 2022-02-11

Published Print: 2022-12

Authors

Malakootian, Mahshid

Jalilian, Masoumeh

Kalayinia, Samira

Hosseini Moghadam, Maryam

Heidarali, Mona

Haghjoo, Majid
Funding

Funding for this research was provided by:

National Institute for Medical Research Development (971510)

Research Deputyship of Rajaie Cardiovascular Medical and Research Center (9774)
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Article History

Received: 27 October 2021

Accepted: 31 January 2022

First Online: 11 February 2022

Declarations

:

: The study protocol was approved by the National Institute for Medical Research Development (NIMAD, 971510) and the Ethics Committee of Rajaie Cardiovascular Medical and Research Center (RHC.AC.IR.REC.1397.088). The study was conducted in accordance with the Helsinki Declaration. All the individuals who joined the study signed written informed consent.

: Not applicable.

: The authors hereby declare no competing interest.

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