Phenotype of cytochrome P4501B1 gene (CYP1B1) mutations in Japanese patients with primary congenital glaucoma

Aim: To investigate the phenotypes associated with cytochrome P4501B1 gene (CYP1B1) mutations in Japanese patients with primary congenital glaucoma (PCG). Methods: 66 Japanese patients with PCG were screened for sequence mutations in the CYP1B1 gene using single strand conformation polymorphism anal...

Полное описание

Сохранить в:
Библиографические подробности
Главные авторы: Ohtake, Y, Tanino, T, Suzuki, Y, Miyata, H, Taomoto, M, Azuma, N, Tanihara, H, Araie, M, Mashima, Y
Формат: Artigo
Язык:Inglês
Опубликовано: Copyright 2003 British Journal of Ophthalmology 2003
Предметы:
Clinical Science
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC1771574/
https://ncbi.nlm.nih.gov/pubmed/12598442
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Схожие документы