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Subject epilepsy -- genetics -- recessive

1. Compound‐heterozygous GRIN2A null variants associated with severe developmental and epileptic encephalopathy. Issue 10 (30th August 2022)

Authors:
Strehlow, Vincent; Rieubland, Claudine; Gallati, Sabina; Kim, Sukhan; Myers, Scott J.; Peterson, Vincent; Ramsey, Amy J.; Teuscher, Daniel D.; Traynelis, Stephen F.; Lemke, Johannes R.
Journal:
Epilepsia
Issue:
Volume 63:Issue 10(2022)
Page Start:
e132
Record Type:
Journal Article
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