Congenital hereditary endothelial dystrophy - mutation analysis of SLC4A11 and genotype-phenotype correlation in a North Indian patient cohort
Preeti Paliwal, Arundhati Sharma, Radhika Tandon, Namrata Sharma, Jeewan S Titiyal, Seema Sen, Tapas C Nag, Rasik B Vajpayee
Molecular Vision | MOLECULAR VISION | Published : 2010
The study was supported by a financial grant provided by the Department of Biotechnology (DBT), India. Financial assistance from the Department of Science and Technology (DST) to the Electron Microscope Facility, AIIMS and Senior Research Fellowship from Council of Scientific and Industrial research (CSIR), India to Preeti Paliwal is gratefully acknowledged.