Homo sapiens retina and anterior neural fold homeobox 2, mRNA (cDNA cl - Nucleotide

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Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease. [Genet Med. 2019]
Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease.
Van de Sompele S, Smith C, Karali M, Corton M, Van Schil K, Peelman F, Cherry T, Rosseel T, Verdin H, Derolez J, et al. Genet Med. 2019 Jun; 21(6):1319-1329. Epub 2018 Oct 31.
TreeGrafter: phylogenetic tree-based annotation of proteins with Gene Ontology terms and other annotations. [Bioinformatics. 2019]
TreeGrafter: phylogenetic tree-based annotation of proteins with Gene Ontology terms and other annotations.
Tang H, Finn RD, Thomas PD. Bioinformatics. 2019 Feb 1; 35(3):518-520.
Autosomal Dominant Retinal Dystrophy With Electronegative Waveform Associated With a Novel RAX2 Mutation. [JAMA Ophthalmol. 2015]
Autosomal Dominant Retinal Dystrophy With Electronegative Waveform Associated With a Novel RAX2 Mutation.
Yang P, Chiang PW, Weleber RG, Pennesi ME. JAMA Ophthalmol. 2015 Jun; 133(6):653-61.

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Homo sapiens retina and anterior neural fold homeobox 2, mRNA (cDNA clone MGC:15...
Homo sapiens retina and anterior neural fold homeobox 2, mRNA (cDNA clone MGC:15631 IMAGE:3344166), complete cds
gi|13938310|gb|BC007284.1|

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