Literature DB >> 31098720

GRIN2A: involvement in movement disorders and intellectual disability without seizures.

Antonio Gennaro Nicotera1, Francesco Calì2, Mirella Vinci2, Sebastiano Antonino Musumeci2.   

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Year:  2019        PMID： 31098720     DOI： 10.1007/s10072-019-03923-2

Source DB:  PubMed          Journal:  Neurol Sci        ISSN： 1590-1874            Impact factor:   3.307


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  5 in total

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2.  wANNOVAR: annotating genetic variants for personal genomes via the web.

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3.  PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine.

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Journal:  Neurology       Date:  2012-10-17       Impact factor: 9.910

4.  GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.

Authors:  Gaetan Lesca; Gabrielle Rudolf; Nadine Bruneau; Natalia Lozovaya; Audrey Labalme; Nadia Boutry-Kryza; Manal Salmi; Timur Tsintsadze; Laura Addis; Jacques Motte; Sukhvir Wright; Vera Tsintsadze; Anne Michel; Diane Doummar; Karine Lascelles; Lisa Strug; Patrick Waters; Julitta de Bellescize; Pascal Vrielynck; Anne de Saint Martin; Dorothee Ville; Philippe Ryvlin; Alexis Arzimanoglou; Edouard Hirsch; Angela Vincent; Deb Pal; Nail Burnashev; Damien Sanlaville; Pierre Szepetowski
Journal:  Nat Genet       Date:  2013-08-11       Impact factor: 38.330

5.  A novel missense mutation in GRIN2A causes a nonepileptic neurodevelopmental disorder.

Authors:  Ana Fernández-Marmiesse; Hirofumi Kusumoto; Saray Rekarte; Iria Roca; Jin Zhang; Scott J Myers; Stephen F Traynelis; Mª Luz Couce; Luis Gutierrez-Solana; Hongjie Yuan
Journal:  Mov Disord       Date:  2018-04-11       Impact factor: 10.338
  5 in total

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