New gene implicated in early-onset generalized dystonia: Lysine-specific methyltransferase 2B (KMT2B)

Sue-Faye Siow¹, Kishore R Kumar^{1

2}

Affiliations

¹ Department of Neurogenetics, Kolling Institute of Medical Research and Royal North Shore Hospital, St Leonards, New South Wales, Australia.
² Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.

Comment

Sue-Faye Siow et al. Mov Disord. 2017 Mar.

. 2017 Mar;32(3):395.

doi: 10.1002/mds.26928. Epub 2017 Feb 2.

Sue-Faye Siow¹, Kishore R Kumar^{1

2}

¹ Department of Neurogenetics, Kolling Institute of Medical Research and Royal North Shore Hospital, St Leonards, New South Wales, Australia.
² Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.

No abstract available

Comment on

Haploinsufficiency of KMT2B, Encoding the Lysine-Specific Histone Methyltransferase 2B, Results in Early-Onset Generalized Dystonia.
Zech M, Boesch S, Maier EM, Borggraefe I, Vill K, Laccone F, Pilshofer V, Ceballos-Baumann A, Alhaddad B, Berutti R, Poewe W, Haack TB, Haslinger B, Strom TM, Winkelmann J. Zech M, et al. Am J Hum Genet. 2016 Dec 1;99(6):1377-1387. doi: 10.1016/j.ajhg.2016.10.010. Epub 2016 Nov 10. Am J Hum Genet. 2016. PMID: 27839873 Free PMC article.