Homo sapiens bromodomain and WD repeat domain containing 3 variant BRW - Nucleotide

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Variants in BRWD3 associated with X-linked partial epilepsy without intellectual disability. [CNS Neurosci Ther. 2023]
Variants in BRWD3 associated with X-linked partial epilepsy without intellectual disability.
Tian MQ, Liu XR, Lin SM, Wang J, Luo S, Gao LD, Chen XB, Liang XY, Liu ZG, He N, et al. CNS Neurosci Ther. 2023 Feb; 29(2):727-735. Epub 2022 Dec 13.
Further clinical and molecular characterization of an XLID syndrome associated with BRWD3 variants, a gene implicated in the leukemia-related JAK-STAT pathway. [Eur J Med Genet. 2023]
Further clinical and molecular characterization of an XLID syndrome associated with BRWD3 variants, a gene implicated in the leukemia-related JAK-STAT pathway.
Delanne J, Lecat M, Blackburn PR, Klee EW, Stumpel CTRM, Stegmann S, Stevens SJC, Nava C, Heron D, Keren B, et al. Eur J Med Genet. 2023 Jan; 66(1):104670. Epub 2022 Nov 19.
Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's disease. [Life Sci Alliance. 2022]
Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's disease.
Viard J, Loe-Mie Y, Daudin R, Khelfaoui M, Plancon C, Boland A, Tejedor F, Huganir RL, Kim E, Kinoshita M, et al. Life Sci Alliance. 2022 Aug 1; 5(12). Epub 2022 Aug 1.

reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome
Order BRWD3 cDNA clone/Protein/Antibody/RNAi [OriGene]
Order BRWD3 cDNA clone/Protein/Antibody/RNAi
OriGene

Homo sapiens bromodomain and WD repeat domain containing 3 variant BRWD3-K (BRWD...
Homo sapiens bromodomain and WD repeat domain containing 3 variant BRWD3-K (BRWD3) mRNA, complete cds, alternatively spliced
gi|42766784|gb|AY497055.1|

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