Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2) von Vithana, Eranga N, Morgan, Patricio, Sundaresan, Periasamy, Ebenezer, Neil D, Tan, Donald T H, Mohamed, Moin D, Anand, Seema, Khine, Khin O, Venkataraman, Divya, Yong, Victor H K, Salto-Tellez, Manuel, Venkatraman, Anandalakshmi, Guo, Ke, Hemadevi, Boomiraj, Srinivasan, Muthiah, Prajna, Venkatesh, Khine, Myint, Casey, Joseph R, Inglehearn, Chris F, Aung, Tin

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Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India von Hemadevi, Boomiraj, Srinivasan, Muthiah, Arunkumar, Jambulingam, Prajna, Namperumalsamy V, Sundaresan, Periasamy

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Human Corneal MicroRNA Expression Profile in Fungal Keratitis von Boomiraj, Hemadevi, Mohankumar, Vidyarani, Lalitha, Prajna, Devarajan, Bharanidharan

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Absence of Phenotype-Genotype Correlation of Patients Expressing Mutations in the SLC4A11 Gene von Mehta, Jodhbir Singh, Hemadevi, Boomiraj, Vithana, Eranga N, Arunkumar, Jambulingam, Srinivasan, Muthaiah, Prajna, Venkatesh, Tan, Donald T, Aung, Tin, Sundaresan, Periasamy

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Identification of Mutations in the SLC4A11 Gene in Patients With Recessive Congenital Hereditary Endothelial Dystrophy von Hemadevi, Boomiraj, Veitia, Reiner A, Srinivasan, Muthiah, Arunkumar, Jambulingam, Prajna, Namperumalsamy Venkatesh, Lesaffre, Corinne, Sundaresan, Periasamy

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