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A novel homozygous splice-site mutation in SCARB2 is associated with progressive myoclonic epilepsy with renal failure

Published Online: 2021-03-26

Published Print: 2021-12

Authors

Yari, Abolfazl

Ali-Nejad, Reza Molla

Saleh-Gohari, Nasrollah https://orcid.org/0000-0003-1256-0323
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Text and Data Mining valid from 2021-03-26

Version of Record valid from 2021-03-26
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Article History

Received: 16 December 2020

Accepted: 16 March 2021

First Online: 26 March 2021

Declarations

:

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

: Our study was approved by the Ethics Committee of the Kerman University of Medical Sciences.

: All family members signed informed consent regarding publishing the clinical data.

: The authors declare no competing interests.

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