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Year | Number of Results |
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2004 | 1 |
2015 | 1 |
2018 | 1 |
2019 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 84839
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Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease.
Genet Med. 2019 Jun;21(6):1319-1329. doi: 10.1038/s41436-018-0345-5. Epub 2018 Oct 31.
Genet Med. 2019.
PMID: 30377383
Free PMC article.
Autosomal Dominant Retinal Dystrophy With Electronegative Waveform Associated With a Novel RAX2 Mutation.
Yang P, Chiang PW, Weleber RG, Pennesi ME.
Yang P, et al.
JAMA Ophthalmol. 2015 Jun;133(6):653-61. doi: 10.1001/jamaophthalmol.2015.0357.
JAMA Ophthalmol. 2015.
PMID: 25789692
Free PMC article.
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QRX, a novel homeobox gene, modulates photoreceptor gene expression.
Wang QL, Chen S, Esumi N, Swain PK, Haines HS, Peng G, Melia BM, McIntosh I, Heckenlively JR, Jacobson SG, Stone EM, Swaroop A, Zack DJ.
Wang QL, et al.
Hum Mol Genet. 2004 May 15;13(10):1025-40. doi: 10.1093/hmg/ddh117. Epub 2004 Mar 17.
Hum Mol Genet. 2004.
PMID: 15028672
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