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Article

A clinical and molecular genetics study of primary congenital glaucoma in South Korea.

The British journal of ophthalmology - 1 Nov 2012

Suh Wool, Kee Changwon

Abstract excerpt

OBJECTIVES: To investigate the clinical manifestations associated with the mutation spectrums of the human cytochrome P450 (CYP1B1) and myocilin (MYOC) genes in South Korean patients with primary congenital glaucoma (PCG). METHODS: Eighty-five unrelated PCG patients and their family members of South Korean origin were screened for mutations in the CYP1B1 and MYOC genes by sequencing with the PCR. We analysed...

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Identifiers

PMID: 22942166
DOI: 10.1136/bjophthalmol-2012-301517

Genes

MYOC

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