Publication | Closed Access
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
Our results confirm the crucial role of CYP1B1 mutations for congenital glaucoma.
| Year | Citations | |
|---|---|---|
Page 1
Page 1