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Comment
. 2023 Sep;25(9):100877.
doi: 10.1016/j.gim.2023.100877. Epub 2023 Jun 5.

Response to Chunquan Cai et al

Silvestre Cuinat  1
Affiliations
Comment

Response to Chunquan Cai et al

Silvestre Cuinat. Genet Med. 2023 Sep.
No abstract available

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest The author declares no conflicts of interest.

Comment on

  • Loss-of-function variants in SRRM2 cause a neurodevelopmental disorder.
    Cuinat S, Nizon M, Isidor B, Stegmann A, van Jaarsveld RH, van Gassen KL, van der Smagt JJ, Volker-Touw CML, Holwerda SJB, Terhal PA, Schuhmann S, Vasileiou G, Khalifa M, Nugud AA, Yasaei H, Ousager LB, Brasch-Andersen C, Deb W, Besnard T, Simon MEH, Amsterdam KH, Verbeek NE, Matalon D, Dykzeul N, White S, Spiteri E, Devriendt K, Boogaerts A, Willemsen M, Brunner HG, Sinnema M, De Vries BBA, Gerkes EH, Pfundt R, Izumi K, Krantz ID, Xu ZL, Murrell JR, Valenzuela I, Cusco I, Rovira-Moreno E, Yang Y, Bizaoui V, Patat O, Faivre L, Tran-Mau-Them F, Vitobello A, Denommé-Pichon AS, Philippe C, Bezieau S, Cogné B. Cuinat S, et al. Genet Med. 2022 Aug;24(8):1774-1780. doi: 10.1016/j.gim.2022.04.011. Epub 2022 May 14. Genet Med. 2022. PMID: 35567594
  • Correspondence on "Loss-of-function variants in SRRM2 cause a neurodevelopmental disorder" by Cuinat et al.
    Sheng W, Yu X, Shu J, Cai C. Sheng W, et al. Genet Med. 2023 Sep;25(9):100878. doi: 10.1016/j.gim.2023.100878. Epub 2023 Jun 5. Genet Med. 2023. PMID: 37272925 No abstract available.