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BOOKS

Books

3 total

Behavioral Phenotype in Five Individuals with De Novo Mutations Within the GRIN2B Gene

Inga Freunscht, Bernt Popp & 11 more

2013

Rescuing Tri-heteromeric NMDA Receptor Function: the Potential of Pregnenolone-sulfate in Loss-of-function GRIN2B Variants

Shai Kellner & Shai Berlin

2024

GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers

Dong Li & Hongjie Yuan & Xilma R. Ortiz-Gonzalez & Eric D. Marsh & Lifeng Tian & Elizabeth M. McCormick & Gabrielle J. Kosobucki & Wenjuan Chen & Anthony J. Schulien & Rosetta Chiavacci & Anel Tankovic & Claudia Naase & Frieder Brueckner & Celina von...

Genres

Books

Behavioral Phenotype in Five Individuals with De Novo Mutations Within the GRIN2B Gene

Rescuing Tri-heteromeric NMDA Receptor Function: the Potential of Pregnenolone-sulfate in Loss-of-function GRIN2B Variants

GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers

Genres

Genres

Books

Behavioral Phenotype in Five Individuals with De Novo Mutations Within the GRIN2B Gene

Rescuing Tri-heteromeric NMDA Receptor Function: the Potential of Pregnenolone-sulfate in Loss-of-function GRIN2B Variants

GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers