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Publications by Sulagna Saitta
Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects
American Journal of Human Genetics
Genetics
A De Novo Mutation Associated With Epilepsy Enhances KV1.2 Voltage Dependence, Suppressing Neuronal Excitability
Biophysical Journal
Biophysics
