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Article

Fine mapping of the Schnyder's crystalline corneal dystrophy locus.

Human genetics - 1 May 2004

Theendakara Veena, Tromp Gerard, Kuivaniemi Helena, White Peter S, Panchal Seema, Cox Jennifer, Winters R Scott, Riebeling Petra, Tost Frank, Hoeltzenbein Maria, Tervo Timo M, Henn Wolfram, Denniger Elke, Krause Matthias, Koksal Murat, Kargi Sebnem, Ugurbas Suat H, Latvala Terho, Shearman Amanda M, Weiss Jayne S

Abstract excerpt

Schnyder's crystalline corneal dystrophy (SCCD) is a rare autosomal dominant eye disease with a spectrum of clinical manifestations that may include bilateral corneal clouding, arcus lipoides, and anterior corneal crystalline cholesterol deposition. We have previously performed a genome-wide linkage analysis on two large Swede-Finn families and mapped the SCCD locus to a 16-cM interval between markers D1S2633 and...

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PMID: 15034782
DOI: 10.1007/s00439-004-1110-1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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Fine mapping of the Schnyder's crystalline corneal dystrophy locus.PMID 15034782Read ↗

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