Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophy von Soumittra, Nagasamy, Loganathan, Sampath K, Madhavan, Dharanija, Ramprasad, Vedam L, Arokiasamy, Tharigopala, Sumathi, Sundaram, Karthiyayini, Thirumalai, Rachapalli, Sudhir R, Kumaramanickavel, Govindasamy, Casey, Joseph R, Rajagopal, Rama

Volltext

High-throughput genetic analysis in a cohort of patients with Ocular Developmental Anomalies von Kandeeban, Suganya, Karthikeyan, Sudha, Thirumalai, Karthiyayini, Swaminathan, Meenakshi, Agarkar, Sumita, Subramian, Nirmala, Sarangapani, Sripriya

Volltext

Prevalence of primary mutations in Leber hereditary optic neuropathy: A five-year report from a tertiary eye care center in India von Sundaramurthy, Srilekha, Selvakumar, Ambika, Dharani, Vidhya, Soumittra, Nagasamy, Mani, Jayaprakash, Thirumalai, Karthiyayini, Periyasamy, Porkodi, Mathavan, Sinnakaruppan, Sripriya, Sarangapani

Volltext

Effect of Curcumin on Lung Resistance-Related Protein (LRP) in Retinoblastoma Cells von Thiyagarajan, Seethalakshmi, Thirumalai, Karthiyayini, Nirmala, Sudarshan, Biswas, Jyotirmay, Krishnakumar, Subramanian

Volltext

Molecular screening of the CYP4V2 gene in Bietti crystalline dystrophy that is associated with choroidal neovascularization von Mamatha, Gandra, Umashankar, Vetrivel, Kasinathan, Nachiappan, Krishnan, Tandava, Sathyabaarathi, Ravichandran, Karthiyayini, Thirumalai, Amali, John, Rao, Chetan, Madhavan, Jagadeesan

Volltext