Associated Papers
Molecular analysis of RAX2-regulated retinal development using human retinal organoids at a single-cell resolution.
Wang S et al.
Frontiers in Cell and Developmental Biology, 2025
Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes.
Hitti-Malin RJ et al.
Biomolecules, 2024
38540785 (PubMed )
Supplement: biomolecules-14-00367-s001.zip › Supplementary_Table_S2-Possibly_and_very_likely_solved_probands.xlsx › Sheet1
Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease.
Van de Sompele S et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
Autosomal Dominant Retinal Dystrophy With Electronegative Waveform Associated With a Novel RAX2 Mutation.
Yang P et al.
Jama Ophthalmology, 2015
Select a paper to view details