glutamate receptor, ionotropic, N-methyl-D-aspartate 3B [Homo sapiens]

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GRIN3B missense mutation as an inherited risk factor for schizophrenia: whole-exome sequencing in a family with a familiar history of psychotic disorders. [Genet Res (Camb). 2017]
GRIN3B missense mutation as an inherited risk factor for schizophrenia: whole-exome sequencing in a family with a familiar history of psychotic disorders.
Hornig T, Grüning B, Kundu K, Houwaart T, Backofen R, Biber K, Normann C. Genet Res (Camb). 2017 Jan 30; 99:e1. Epub 2017 Jan 30.
Novel and rare functional genomic variants in multiple autoimmune syndrome and Sjögren's syndrome. [J Transl Med. 2015]
Novel and rare functional genomic variants in multiple autoimmune syndrome and Sjögren's syndrome.
Johar AS, Mastronardi C, Rojas-Villarraga A, Patel HR, Chuah A, Peng K, Higgins A, Milburn P, Palmer S, Silva-Lara MF, et al. J Transl Med. 2015 Jun 2; 13:173. Epub 2015 Jun 2.
A naturally occurring null variant of the NMDA type glutamate receptor NR3B subunit is a risk factor of schizophrenia. [PLoS One. 2015]
A naturally occurring null variant of the NMDA type glutamate receptor NR3B subunit is a risk factor of schizophrenia.
Matsuno H, Ohi K, Hashimoto R, Yamamori H, Yasuda Y, Fujimoto M, Yano-Umeda S, Saneyoshi T, Takeda M, Hayashi Y. PLoS One. 2015; 10(3):e0116319. Epub 2015 Mar 13.

RefSeq protein
See the reference protein sequence for glutamate receptor ionotropic, NMDA 3B precursor (NP_619635.1).

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glutamate receptor, ionotropic, N-methyl-D-aspartate 3B [Homo sapiens]
glutamate receptor, ionotropic, N-methyl-D-aspartate 3B [Homo sapiens]
gi|119589982|gb|EAW69576.1||gnl|WGS |hCP1801636

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