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Comment
. 2023 May;38(5):911-913.
doi: 10.1002/mds.29384.

Reply to: Early-Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST

Afshin Saffari  1 , Darius Ebrahimi-Fakhari  1
Affiliations
Comment

Reply to: Early-Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST

Afshin Saffari et al. Mov Disord. 2023 May.
No abstract available

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Conflict of interest statement

Relevant conflicts of interest/financial disclosures: None.

Comment on

References

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    1. Alecu JE, Saffari A, Jumo H, et al. Novel CAPN1 missense variants in complex hereditary spastic paraplegia with early-onset psychosis. Ann Clin Transl Neurol 2022;9(4):570–576. - PMC - PubMed
    1. Alecu JE, Saffari A, Jordan C, Srivastava S, Blackstone C, Ebrahimi-Fakhari D. De novo variants cause complex symptoms in HSP-ATL1 (SPG3A) and uncover genotype-phenotype correlations. Hum Mol Genet 2022. - PMC - PubMed
    1. Saffari A, Kellner M, Jordan C, et al. The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15. Brain 2022. - PMC - PubMed
    1. Ebrahimi-Fakhari D, Teinert J, Behne R, et al. Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia. Brain 2020;143(10):2929–2944. - PMC - PubMed