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Comment
. 2022 Dec;37(12):2466-2467.
doi: 10.1002/mds.29256.

Reply to: "GNAO1 Haploinsufficiency Associated with a Mild Delayed-Onset Dystonia Phenotype"

Thomas Wirth  1   2   3 , Giacomo Garone  4   5 , Manju A Kurian  6 , Amélie Piton  2   3   7 , Emmanuel Roze  8   9 , Jean Pierre Lin  10   11 , Christine Tranchant  1   2   3 , Laura Cif  12 , Diane Doummar  13 , Mathieu Anheim  1   2   3
Affiliations
Comment

Reply to: "GNAO1 Haploinsufficiency Associated with a Mild Delayed-Onset Dystonia Phenotype"

Thomas Wirth et al. Mov Disord. 2022 Dec.
No abstract available

PubMed Disclaimer

Comment on

  • Highlighting the Dystonic Phenotype Related to GNAO1.
    Wirth T, Garone G, Kurian MA, Piton A, Millan F, Telegrafi A, Drouot N, Rudolf G, Chelly J, Marks W, Burglen L, Demailly D, Coubes P, Castro-Jimenez M, Joriot S, Ghoumid J, Belin J, Faucheux JM, Blumkin L, Hull M, Parnes M, Ravelli C, Poulen G, Calmels N, Nemeth AH, Smith M, Barnicoat A, Ewenczyk C, Méneret A, Roze E, Keren B, Mignot C, Beroud C, Acosta F Jr, Nowak C, Wilson WG, Steel D, Capuano A, Vidailhet M, Lin JP, Tranchant C, Cif L, Doummar D, Anheim M. Wirth T, et al. Mov Disord. 2022 Jul;37(7):1547-1554. doi: 10.1002/mds.29074. Epub 2022 Jun 20. Mov Disord. 2022. PMID: 35722775 Free PMC article.
  • GNAO1 Haploinsufficiency Associated with a Mild Delayed-Onset Dystonia Phenotype.
    Krenn M, Sommer R, Sycha T, Zech M. Krenn M, et al. Mov Disord. 2022 Dec;37(12):2464-2466. doi: 10.1002/mds.29258. Epub 2022 Oct 23. Mov Disord. 2022. PMID: 36273395 No abstract available.

References

    1. Krenn M, Sommer R, Sycha T, Zech M. GNAO1 haploinsufficiency associated with a mild delayed-onset dystonia phenotype. Mov Disord 2022;37(12):2464-2466. https://doi.org/10.1002/mds.29258
    1. Wirth T, Garone G, Kurian MA, Piton A, Millan F, Telegrafi A, et al. Highlighting the dystonic phenotype related to GNAO1. Mov Disord 2022;37(7):1547-1554.
    1. Lasa-Aranzasti A, Cazurro-Gutiérrez A, Bescós A, González V, Ispierto L, Tardáguila M, et al. 16q12.2q21 deletion: a newly recognized cause of dystonia related to GNAO1 haploinsufficiency. Parkinsonism Relat. Disord 2022;103:112-114.
    1. Feng H, Khalil S, Neubig RR, Sidiropoulos C. A mechanistic review on GNAO1-associated movement disorder. Neurobiol Dis 2018;116:131-141.
    1. Muntean BS, Masuho I, Dao M, Sutton LP, Zucca S, Iwamoto H, et al. Gαo is a major determinant of cAMP signaling in the pathophysiology of movement disorders. Cell Rep 2021;34(5):108718.

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