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Pathogenic variants in KPTN gene identified by clinical whole-genome sequencing.
Thiffault I, Atherton A, Heese BA, T Abdelmoity A, Pawar K, Farrow E, Zellmer L, Miller N, Soden S, Saunders C. Thiffault I, et al. Among authors: atherton a. Cold Spring Harb Mol Case Stud. 2020 Jun 12;6(3):a003970. doi: 10.1101/mcs.a003970. Print 2020 Jun. Cold Spring Harb Mol Case Stud. 2020. PMID: 32358097 Free PMC article.
HSP and deafness: Neurocristopathy caused by a novel mosaic SOX10 mutation.
Donkervoort S, Bharucha-Goebel D, Yun P, Hu Y, Mohassel P, Hoke A, Zein WM, Ezzo D, Atherton AM, Modrcin AC, Dasouki M, Foley AR, Bönnemann CG. Donkervoort S, et al. Among authors: atherton am. Neurol Genet. 2017 May 15;3(3):e151. doi: 10.1212/NXG.0000000000000151. eCollection 2017 Jun. Neurol Genet. 2017. PMID: 28534044 Free PMC article.
67 results