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Article

Fine mapping of chromosome 9 locus associated with congenital cataract.

International ophthalmology - 1 Jun 2018

Kaul Haiba, Hussain Shabbir, Mustafa Ghulam, Naz Shagufta

Abstract excerpt

PURPOSE: The purpose of this study was to study the molecular basis of inherited autosomal recessive cataracts in Pakistan population and to identify the molecular defect segregating with the disease phenotype. METHODS: Families having two or more affected individuals were identified through hospital, blood samples were collected and DNA was extracted. We employed the traditional strategy of linkage analysis...

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PMID: 28585112
DOI: 10.1007/s10792-017-0581-8

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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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