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   Luyao Zhu et al, 2021, Ophthalmic Genetics CrossRef
2. Genotype-phenotype associations in CRB1 bi-allelic patients: a novel mutation, a systematic review and meta-analysis
   Ahmad Daher et al, 2024, BMC Ophthalmology CrossRef
3. Retinal capillaritis in a CRB1-associated retinal dystrophy
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5. CRB1-Associated Retinal Dystrophies: Genetics, Clinical Characteristics, and Natural History
   Malena Daich Varela et al, 2023, American Journal of Ophthalmology CrossRef
6. Clinical and Genetic Analysis of 63 Families Demonstrating Early and Advanced Characteristic Fundus as the Signature of CRB1 Mutations
   Yingwei Wang et al, 2021, American Journal of Ophthalmology CrossRef
7. Protein O-Glucosyltransferase 1 (POGLUT1) Promotes Mouse Gastrulation through Modification of the Apical Polarity Protein CRUMBS2
   Nitya Ramkumar et al, 2015, PLOS Genetics CrossRef
8. CERKL mutation causing retinitis pigmentosa(RP) in Indian population – a genotype and phenotype correlation study
   Parveen Sen et al, 2020, Ophthalmic Genetics CrossRef
9. Molecular genetics of Leber congenital amaurosis in Chinese: New data from 66 probands and mutation overview of 159 probands
   Yan Xu et al, 2016, Experimental Eye Research CrossRef