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Observation of nine previously reported and 10 non-reported SLC4A11 mutations among 20 Iranian CHED probands and identification of an MPDZ mutation as possible cause of CHED and FECD in one family
Moazzeni, Hamidreza, Javadi, Mohammad Ali, Asgari, Danial, Khani, Marzieh, Emami, Mohammad, Moghadam, Abolfazl, Panahi-Bazaz, Mahmoud-Reza, Hosseini Tehrani, Mehdi, Karimian, Farid, Hosseini, Bagher,Language:
english
Journal:
British Journal of Ophthalmology
DOI:
10.1136/bjophthalmol-2019-314377
Date:
August, 2019
File:
PDF, 1.29 MB
english, 2019