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Case Reports
. 2019 Mar-Apr;67(2):562-563.
doi: 10.4103/0028-3886.257986.

Novel GRIN2B mutation: A rare cause of severe epileptic encephalopathy

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Free article
Case Reports

Novel GRIN2B mutation: A rare cause of severe epileptic encephalopathy

Indar Kumar Sharawat et al. Neurol India. 2019 Mar-Apr.
Free article
No abstract available

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