Associated Papers
Novel mutations in LTBP2 identified in familial cases of primary congenital glaucoma.
Rauf B et al.
Molecular Vision, 2020
Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma.
Micheal S et al.
Plos One, 2016
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