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المؤلفون: Myint Khine, Donald T.H. Tan, Khin O Khine, Muthiah Srinivasan, Chris F. Inglehearn, Moin D. Mohamed, Victor H. K. Yong, Venkatesh N Prajna, Periasamy Sundaresan, Neil D. Ebenezer, Boomiraj Hemadevi, Tin Aung, Anandalakshmi Venkatraman, Patricio E. Morgan, Joseph R. Casey, Ke Guo, Eranga N. Vithana, Seema Anand, Manuel Salto-Tellez, Divya Venkataraman
المصدر: Nature genetics. 38(7)
مصطلحات موضوعية: Male, genetic structures, Endothelium, Anion Transport Proteins, Corneal dystrophy, Genes, Recessive, Biology, medicine.disease_cause, Antiporters, Borates, Genetics, medicine, Humans, Point Mutation, Gene, Loss function, Corneal Dystrophies, Hereditary, Mutation, Fuchs' Endothelial Dystrophy, Dystrophy, medicine.disease, Molecular biology, eye diseases, medicine.anatomical_structure, Amino Acid Substitution, Cancer research, Female, sense organs, Congenital hereditary endothelial dystrophy, Cotransporter