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Article

CYP1B1 gene mutations causing primary congenital glaucoma in Tunisia.

Annals of human genetics - 1 Jul 2014

Bouyacoub Yosra, Ben Yahia Salim, Abroug Nesrine, Kahloun Rim, Kefi Rym, Khairallah Moncef, Abdelhak Sonia

Abstract excerpt

Primary congenital glaucoma (PCG) is responsible for a significant proportion of childhood blindness in Tunisia. Early prevention based on genetic diagnosis is therefore required. This study sought to determine the frequency of CYP1B1 (cytochrome P450, family 1, subfamily B, polypeptide 1) mutations in 18 PCG patients, recruited from Central and Southern of Tunisia. Genomic DNA was extracted and the coding...

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Identifiers

PMID: 24942078
DOI: 10.1111/ahg.12069

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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