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Summary Literature (1)
Literature for OMIM 614618: HYPEREKPLEXIA 3; HKPX3


Xenbase Articles:
( Denotes literature images)
GlyT1 encephalopathy: Characterization of presumably disease causing GlyT1 mutations., Hauf K,Barsch L,Bauer D,Buchert R,Armbruster A,Frauenfeld L,Grasshoff U,Eulenburg V, Neurochem Int. October 1, 2020; 139:1872-9754.