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[Loss of heterozygosity at microsatellite marker localised near the metalloproteinase gene in patients with PEX syndrome].

Authors
  • Zalewska, Renata
  • Mariak, Zofia
  • Pepiński, Witold
  • Wojnar, Małgorzata
  • Proniewska-Skretek, Ewa
  • Skawrońska, Małgorzata
  • Janica, Jerzy
Type
Published Article
Journal
Klinika oczna
Publication Date
Jan 01, 2004
Volume
106
Issue
1-2 Suppl
Pages
153–154
Identifiers
PMID: 15510480
Source
Medline
License
Unknown

Abstract

The high frequency of LOH in PEX patients at locus D7S820 suggests that genetic factors may be involved in the etiology and pathogenesis of PEX.

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