Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleNovel PHKA1 mutation in glycogen storage disease type IXD with typical myotonic discharges.AuthorsWang, Cong‐Cong; Yang, Bing; Liu, Ying; Li, Xiao‐Li; Liu, Bin; Duan, Rui‐ShengPublicationCNS Neuroscience & Therapeutics, 2022, Vol 28, Issue 11, p1895ISSN1755-5930Publication typeArticleDOI10.1111/cns.13939