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Comment
. 2018 Feb;83(2):439.
doi: 10.1002/ana.25154.

Reply to "a novel mutation in the transmembrane 6 domain of GABBR2 leads to a rett-like phenotype"

Yongjin Yoo  1 , Jaeso Cho  1 , Murim Choi  1
Affiliations
Comment

Reply to "a novel mutation in the transmembrane 6 domain of GABBR2 leads to a rett-like phenotype"

Yongjin Yoo et al. Ann Neurol. 2018 Feb.
No abstract available

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Comment on

  • GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathy.
    Yoo Y, Jung J, Lee YN, Lee Y, Cho H, Na E, Hong J, Kim E, Lee JS, Lee JS, Hong C, Park SY, Wie J, Miller K, Shur N, Clow C, Ebel RS, DeBrosse SD, Henderson LB, Willaert R, Castaldi C, Tikhonova I, Bilgüvar K, Mane S, Kim KJ, Hwang YS, Lee SG, So I, Lim BC, Choi HJ, Seong JY, Shin YB, Jung H, Chae JH, Choi M. Yoo Y, et al. Ann Neurol. 2017 Sep;82(3):466-478. doi: 10.1002/ana.25032. Ann Neurol. 2017. PMID: 28856709
  • A novel mutation in the transmembrane 6 domain of GABBR2 leads to a Rett-like phenotype.
    Vuillaume ML, Jeanne M, Xue L, Blesson S, Denommé-Pichon AS, Alirol S, Brulard C, Colin E, Isidor B, Gilbert-Dussardier B, Odent S, Parent P, Donnart A, Redon R, Bézieau S, Rondard P, Laumonnier F, Toutain A. Vuillaume ML, et al. Ann Neurol. 2018 Feb;83(2):437-439. doi: 10.1002/ana.25155. Epub 2018 Feb 7. Ann Neurol. 2018. PMID: 29369404 No abstract available.

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