SPTAN1 variants likely cause autosomal recessive complicated hereditary spastic paraplegia
Crossref DOI link: https://doi.org/10.1038/s10038-021-00975-1
Published Online: 2021-09-16
Published Print: 2022-03
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Xie, Fei
Chen, Shuqi
Liu, Peng
Chen, Xinhui
Luo, Wei http://orcid.org/0000-0001-6951-7698
Text and Data Mining valid from 2021-09-16
Version of Record valid from 2021-09-16
Article History
Received: 23 June 2021
Revised: 24 August 2021
Accepted: 24 August 2021
First Online: 16 September 2021
Competing interests
: The authors declare no competing interests.