Identification of a Novel ZNF469 Mutation in a Pakistani...

Identification of a Novel ZNF469 Mutation in a Pakistani Family With Brittle Cornea Syndrome

Micheal, Shazia, Siddiqui, Sorath Noorani, Zafar, Saemah Nuzhat, Gabriëla Niewold, Ilse Therésia, Khan, Muhammad Imran, Bergen, Arthur A. B.
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Volume:
38
Journal:
Cornea
DOI:
10.1097/ico.0000000000001828
Date:
June, 2019
File:
PDF, 506 KB
2019
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