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MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia

Published Online: 2022-06-15

Published Print: 2022-07

Authors

Selçuk, Ece

Kırımtay, Koray

Temizci, Benan

Akarsu, Şeyma

Everest, Elif

Baslo, Mehmet Barış

Demirkıran, Meltem

Yapıcı, Zuhal

Karabay, Arzu https://orcid.org/0000-0001-5150-5349
Funding

Funding for this research was provided by:

Istanbul Teknik Üniversitesi (1239-39586)
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Text and Data Mining valid from 2022-06-15

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Article History

Received: 20 January 2022

Accepted: 23 May 2022

First Online: 15 June 2022

Declarations

:

: Authors do not have any conflict of interest.

: Ethical approval was obtained by the Ethics Committee of Istanbul Technical University and Biruni University Hospital.

: Informed consent was obtained from all participants included in the study.

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