Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11
Jiao, X. Sultana, A. Garg, P. Ramamurthy, B. Vemuganti, G.K. Gangopadhyay, N. Hejtmancik, J.F. Kannabiran, C.
Journal of Medical Genetics, 2007
https://doi.org/10.1136/jmg.2006.044644
Chitra Kannabiran
Kannabiran Chitra / Kannabiran C
ORCID: 0000-0001-8435-0320
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Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11 10.1136/jmg.2006.044644
Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract. 10.1136/jmg.2007.050138
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TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients 10.1167/iovs.04-0440
Prashant Garg
Garg Prashant
ORCID: 0000-0003-4989-2815
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Microsporidial keratitis in India: 16s rRNA gene-based PCR assay for diagnosis and species identification of microsporidia in clinical samples 10.1167/iovs.06-0376
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Erratum: Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11 (Journal of Medical Genetics (2007) 44, (64-68)) 10.1136/jmg.2006.044644corr1
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Authors reply 10.1093/SW/25.4.335-A
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Response to ‘Comment on: ‘A randomized masked pilot clinical trial to compare the efficacy of topical 1% Voriconazole ophthalmic solution as monotherapy to combination therapy with topical 0.02% Polyhexamethylene biguanide and 0.02% Chlorhexidine in the treatment of Acanthamoeba keratitis’’ 10.1038/s41433-021-01401-8
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