Missense mutation inSLC4A11in two Pakistani families affected with congenital hereditary endothelial dystrophy (CHED2)

Haiba Kaul, Maryam Suman, Zoya Khan, Muhammad Ikram Ullah, Usman Ali Ashfaq, Sobia Idrees
  • Clinical and Experimental Optometry, August 2015, Wiley
  • DOI: 10.1111/cxo.12276
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