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Primary Congenital Glaucoma: A Novel Single-Nucleotide Deletion and Varying Phenotypic Expression for the 1546???1555dup Mutation in the GLC3A (CYP1B1) Gene in 2 Families of Different Ethnic Origin

33

Citations

11

References

2003

Year

Abstract

Our results confirm the crucial role of CYP1B1 mutations for congenital glaucoma.

References

YearCitations

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