H.sapiens DNA for ORF1 and ORF2 from chromosome X

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Investigating the Impact of Dimer Interface Mutations on Norrin's Secretion and Norrin/β-Catenin Pathway Activation. [Invest Ophthalmol Vis Sci. 2024]
Investigating the Impact of Dimer Interface Mutations on Norrin's Secretion and Norrin/β-Catenin Pathway Activation.
Liu M, Dai E, Yang M, Li S, Fan L, Liu Y, Xiao H, Zhao P, Yang Z. Invest Ophthalmol Vis Sci. 2024 Mar 5; 65(3):31.
Novel mutation in the NDP gene associated with Norrie disease in a Chinese pedigree. [Mol Genet Genomic Med. 2024]
Novel mutation in the NDP gene associated with Norrie disease in a Chinese pedigree.
Jiang K, Wang S, Sun H, Peng C, Li N, Li S, Gao R, Zhang J. Mol Genet Genomic Med. 2024 Jan; 12(1):e2345. Epub 2023 Dec 26.
Whole exome sequencing revealed novel pathogenic variants in Vietnamese patients with FEVR. [Mol Vis. 2022]
Whole exome sequencing revealed novel pathogenic variants in Vietnamese patients with FEVR.
Trang DT, Phu NM, Hung DM, Nhung VP, Ha NN, Thuong MTH, Ngoc TTB, Hiep NX, Ton ND, Hai NV, et al. Mol Vis. 2022; 28:480-491. Epub 2022 Dec 21.

H.sapiens DNA for ORF1 and ORF2 from chromosome X
H.sapiens DNA for ORF1 and ORF2 from chromosome X
gi|29946|emb|X65724.1|

Nucleotide

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Nucleotide