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Page 1
Identification of a Novel ZNF469 Mutation in a Pakistani Family With Brittle Cornea Syndrome.
Cornea. 2019 Jun;38(6):718-722. doi: 10.1097/ICO.0000000000001828.
Cornea. 2019.
PMID: 30865045
Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families.
Micheal S, Niewold ITG, Siddiqui SN, Zafar SN, Khan MI, Bergen AAB.
Micheal S, et al. Among authors: niewold itg.
Genes (Basel). 2018 Feb 20;9(2):112. doi: 10.3390/genes9020112.
Genes (Basel). 2018.
PMID: 29461512
Free PMC article.
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