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23. Whole Exome Sequencing in Eight Thai Patients With Leber Congenital Amaurosis Reveals Mutations in the CTNNA1 and CYP4V2 Genes. Jinda W; Taylor TD; Suzuki Y; Thongnoppakhun W; Limwongse C; Lertrit P; Trinavarat A; Atchaneeyasakul LO Invest Ophthalmol Vis Sci; 2017 Apr; 58(4):2413-2420. PubMed ID: 28453600 [TBL] [Abstract][Full Text] [Related]
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