Literature DB >> 31085877

Novel GRIN2B mutation: A rare cause of severe epileptic encephalopathy.

Indar Kumar Sharawat1, Jaivinder Yadav1, Lokesh Saini1.   

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Year:  2019        PMID： 31085877     DOI： 10.4103/0028-3886.257986

Source DB:  PubMed          Journal:  Neurol India        ISSN： 0028-3886            Impact factor:   2.117


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  2 in total

1.  CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders.

Authors:  Prateek K Panda; Radhapyari Lourembam; Indar K Sharawat
Journal:  Ann Indian Acad Neurol       Date:  2021-02-04       Impact factor: 1.383

Review 2.  Roles of N-Methyl-D-Aspartate Receptors (NMDARs) in Epilepsy.

Authors:  Shuang Chen; Da Xu; Liu Fan; Zhi Fang; Xiufeng Wang; Man Li
Journal:  Front Mol Neurosci       Date:  2022-01-07       Impact factor: 5.639
  2 in total

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