CYP1B1 mutations in patients with primary congenital glaucoma from Saudi Arabia

BACKGROUND: CYP1B1 is the most commonly mutated gene in primary congenital glaucoma (PCG). This study was undertaken to identify mutations in CYP1B1 in the Western region of Saudi Arabia. METHODS: Blood of patients who had typical findings of PCG, were screened by direct sequencing of all coding exo...

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Detalles Bibliográficos
Autores principales: Badeeb, Osama M, Micheal, Shazia, Koenekoop, Robert K, den Hollander, Anneke I, Hedrawi, Manal T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4258803/
https://www.ncbi.nlm.nih.gov/pubmed/25261878
http://dx.doi.org/10.1186/s12881-014-0109-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4258803/
https://www.ncbi.nlm.nih.gov/pubmed/25261878
http://dx.doi.org/10.1186/s12881-014-0109-2

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