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A novel mutation in HINT1 gene causes autosomal recessive axonal neuropathy with neuromyotonia, effective treatment with carbamazepine and review of the literature

Crossref DOI link: https://doi.org/10.1007/s13760-022-02006-y

Published Online: 2022-06-29

Published Print: 2022-10

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Xu, Ling

Wang, Guangyu

Lv, Xiaoqing

Zhang, Dong

Yan, Chuanzhu

Lin, Pengfei https://orcid.org/0000-0002-0861-5785
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Text and Data Mining valid from 2022-06-29

Version of Record valid from 2022-06-29
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Article History

Received: 17 December 2021

Accepted: 9 June 2022

First Online: 29 June 2022

Declarations

:

: This study was in compliance with the Declaration of Helsinki and approved by the Ethics Committee of Shandong University School of Medicine.

: Informed consent was provided by the patient and parents.

: The authors declare that they have no competing interests.

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