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Summary Literature (1)
Literature for DOID 0050526: Gamstorp-Wohlfart syndrome


Xenbase Articles :
( Denotes literature images)
Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia., Chen H,von Hehn C,Kaczmarek LK,Ment LR,Pober BR,Hisama FM, Neurogenetics. April 1, 2007; 8(2):1364-6745.