CYP1B1-Related Anterior Segment Developmental Anomalies

Author:

Kelberman Daniel,Islam Lily,Jacques Thomas S.,Russell-Eggitt Isabelle,Bitner-Glindzicz Maria,Khaw Peng T.,Nischal Ken K.,Sowden Jane C.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference31 articles.

1. Null mutations in LTBP2 cause primary congenital glaucoma;Ali;Am J Hum Genet,2009

2. Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma;Narooie-Nejad;Hum Mol Genet,2009

3. Novel CYP1B1 mutations in consanguineous Pakistani families with primary congenital glaucoma;Firasat;Mol Vis [serial online],2008

4. Investigation of CYP1B1 mutations in Chinese patients with primary congenital glaucoma;Yang;Mol Vis [serial online],2009

5. A clinical and molecular genetic study of German patients with primary congenital glaucoma;Weisschuh;Am J Ophthalmol,2009

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