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Mutation screening of the CYP1B1 gene reveals thirteen novel disease-causing variants in consanguineous Pakistani families causing primary congenital glaucoma

Table 1

List of reported and novel disease-causing variants detected in this study upon sequencing of CYP1B1 gene in PCG patients.

Table 1

doi: https://doi.org/10.1371/journal.pone.0274335.t001