Reply to: "α-Synuclein (SNCA) A30G Mutation as a Cause of a Complex Phenotype Without Parkinsonism"

Hui Liu¹, Christos Koros^{2

3}, Leonidas Stefanis^{2

4}, Thomas Gasser¹

Affiliations

¹ Department for Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen and German Center of Neurodegenerative Diseases (DZNE), Tübingen, Germany.
² 1st Department of Neurology, Eginition Hospital, National and Kapodistrian University of Athens, Athens, Greece.
³ 2nd Department of Neurology, Attikon Hospital, National and Kapodistrian University of Athens, Athens, Greece.
⁴ Laboratory of Neurodegenerative Diseases, Biomedical Research Foundation of the Academy of Athens, Athens, Greece.

Comment

Hui Liu et al. Mov Disord. 2021 Sep.

. 2021 Sep;36(9):2212-2213.

doi: 10.1002/mds.28742.

Hui Liu¹, Christos Koros^{2

3}, Leonidas Stefanis^{2

4}, Thomas Gasser¹

¹ Department for Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen and German Center of Neurodegenerative Diseases (DZNE), Tübingen, Germany.
² 1st Department of Neurology, Eginition Hospital, National and Kapodistrian University of Athens, Athens, Greece.
³ 2nd Department of Neurology, Attikon Hospital, National and Kapodistrian University of Athens, Athens, Greece.
⁴ Laboratory of Neurodegenerative Diseases, Biomedical Research Foundation of the Academy of Athens, Athens, Greece.

No abstract available

Comment on

A Novel SNCA A30G Mutation Causes Familial Parkinson's Disease.
Liu H, Koros C, Strohäker T, Schulte C, Bozi M, Varvaresos S, Ibáñez de Opakua A, Simitsi AM, Bougea A, Voumvourakis K, Maniati M, Papageorgiou SG, Hauser AK, Becker S, Zweckstetter M, Stefanis L, Gasser T. Liu H, et al. Mov Disord. 2021 Jul;36(7):1624-1633. doi: 10.1002/mds.28534. Epub 2021 Feb 22. Mov Disord. 2021. PMID: 33617693
α-Synuclein (SNCA) A30G Mutation as a Cause of a Complex Phenotype Without Parkinsonism.
Sokratous M, Breza M, Senkevich K, Gan-Or Z, Kalampokini S, Spanaki C, Provatas A, Zaunmuktane Z, Valotassiou V, Georgoulias P, Efthymiou S, Hadjigeorgiou GM, Houlden H, Xiromerisiou G. Sokratous M, et al. Mov Disord. 2021 Sep;36(9):2209-2212. doi: 10.1002/mds.28735. Mov Disord. 2021. PMID: 34543462 No abstract available.

1. Sokratous M, Breza M, Senkevich K, et al. Alpha-synuclein (SNCA) A30G mutation as a cause of a complex phenotype without parkinsonism. Mov Disord 2021. in press.
1. Liu H, Koros C, Strohäker T, et al. A novel SNCA A30G mutation causes familial Parkinson's disease. Mov Disord 2021;36(7):1624-1633. https://doi.org/10.1002/mds.28534
1. Stenton SL, Prokisch H. Genetics of mitochondrial diseases: identifying mutations to help diagnosis. EBioMedicine 2020;56:102784.