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Article

Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping.

International journal of molecular medicine - 1 Apr 2008

Nürnberg Gudrun, Jacobi Felix K, Broghammer Martina, Becker Christian, Blin Nikolaus, Nürnberg Peter, Stephani Ulrich, Pusch Carsten M

Abstract excerpt

Myopia, or short-sightedness, is the most common form of vision disorder worldwide. Higher levels of myopia, usually defined as an axial eye length of >26 mm or a refractive error of < -5.00 diopters are often designated as 'pathologic' myopia, because of the predisposition to develop further eye...

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PMID: 18360688

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18360688-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping.PMID 18360688Read ↗

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Fine mapping linkage analysis identifies a novel susceptibility locus for myopia on chromosome 2q37 adjacent to but not overlapping MYP12.Semantic proximity Read ↗

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.Semantic proximity Read ↗

A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612.Semantic proximity Read ↗

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