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2. Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts. Irum B; Khan SY; Ali M; Kaul H; Kabir F; Rauf B; Fatima F; Nadeem R; Khan AO; Al Obaisi S; Naeem MA; Nasir IA; Khan SN; Husnain T; Riazuddin S; Akram J; Eghrari AO; Riazuddin SA PLoS One; 2016; 11(11):e0162620. PubMed ID: 27814360 [TBL] [Abstract][Full Text] [Related]
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4. A missense mutation in the LIM2 gene is associated with autosomal recessive presenile cataract in an inbred Iraqi Jewish family. Pras E; Levy-Nissenbaum E; Bakhan T; Lahat H; Assia E; Geffen-Carmi N; Frydman M; Goldman B; Pras E Am J Hum Genet; 2002 May; 70(5):1363-7. PubMed ID: 11917274 [TBL] [Abstract][Full Text] [Related]
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6. A novel missense mutation in Berry V; Pontikos N; Dudakova L; Moore AT; Quinlan R; Liskova P; Michaelides M Ophthalmic Genet; 2020 Apr; 41(2):131-134. PubMed ID: 32202185 [No Abstract] [Full Text] [Related]
7. Lim2(To3) transgenic mice establish a causative relationship between the mutation identified in the lim2 gene and cataractogenesis in the To3 mouse mutant. Steele EC; Wang JH; Lo WK; Saperstein DA; Li X; Church RL Mol Vis; 2000 Jun; 6():85-94. PubMed ID: 10851259 [TBL] [Abstract][Full Text] [Related]
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9. Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract. Ponnam SP; Ramesha K; Tejwani S; Ramamurthy B; Kannabiran C J Med Genet; 2007 Jul; 44(7):e85. PubMed ID: 17601931 [TBL] [Abstract][Full Text] [Related]
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19. Identification of a mutation in the MP19 gene, Lim2, in the cataractous mouse mutant To3. Steele EC; Kerscher S; Lyon MF; Glenister PH; Favor J; Wang J; Church RL Mol Vis; 1997 May; 3():5. PubMed ID: 9238094 [TBL] [Abstract][Full Text] [Related]
20. Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea. Devi RR; Vijayalakshmi P Mol Vis; 2006 Mar; 12():190-5. PubMed ID: 16604058 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]