Homo sapiens clarin-1 transcript variant 10 (CLRN1) mRNA, partial cds, - Nucleotide

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Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf Cohort. [Invest Ophthalmol Vis Sci. 2022]
Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf Cohort.
Smirnov VM, Nassisi M, Mohand-Saïd S, Bonnet C, Aubois A, Devisme C, Dib T, Zeitz C, Loundon N, Marlin S, et al. Invest Ophthalmol Vis Sci. 2022 Apr 1; 63(4):25.
A reference map of the human binary protein interactome. [Nature. 2020]
A reference map of the human binary protein interactome.
Luck K, Kim DK, Lambourne L, Spirohn K, Begg BE, Bian W, Brignall R, Cafarelli T, Campos-Laborie FJ, Charloteaux B, et al. Nature. 2020 Apr; 580(7803):402-408. Epub 2020 Apr 8.
Extending the spectrum of CLRN1- and ABCA4-associated inherited retinal dystrophies caused by novel and recurrent variants using exome sequencing. [Mol Genet Genomic Med. 2020]
Extending the spectrum of CLRN1- and ABCA4-associated inherited retinal dystrophies caused by novel and recurrent variants using exome sequencing.
Abu-Ameerh M, Mohammad H, Dardas Z, Barham R, Ali D, Bijawi M, Tawalbeh M, Amr S, Hatmal MM, Al-Bdour M, et al. Mol Genet Genomic Med. 2020 Mar; 8(3):e1123. Epub 2020 Jan 22.