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A rare TNNT1 gene variant causing creatine kinase elevation in nemaline myopathy: c.271_273del (p.Lys91del)

Published Online: 2024-02-16

Published Print: 2024-05

Authors

Yavaş, Cüneyd http://orcid.org/0000-0002-1597-5922
Doğan, Mustafa

Eröz, Recep

Türegün, Kübra
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Text and Data Mining valid from 2024-02-16

Version of Record valid from 2024-02-16
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Article History

Received: 1 December 2023

Accepted: 1 February 2024

First Online: 16 February 2024

Declarations

:

: All authors have no relevant financial or nonfinancial interests to disclose.

: Informed consent forms for medical examinations, and genetic analysis were obtained from all participants and their legal representatives; the procedures were conducted in accordance with the Helsinki Declaration, and the Ethics Committee of Hospital approved the relevant studies (KAEK/16.08.2023.357).

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