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pro vyhledávání: '"Periasamy Sundaresan"'
Autor:
Namperumalsamy Venkatesh Prajna, Reiner A. Veitia, Jambulingam Arunkumar, Boomiraj Hemadevi, Corinne Lesaffre, Muthiah Srinivasan, Periasamy Sundaresan
Publikováno v:
Archives of Ophthalmology. 126:700
Objective To identify Solute Carrier family 4 (sodium borate cotransporter) member 11 ( SLC4A11 ) gene mutations associated with autosomal recessive congenital hereditary endothelial dystrophy (CHED2). Methods DNA extraction from blood, polymerase ch