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 PMID:17356513  

Retinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4.

Anne McMahon | Igor A Butovich | Nathan L Mata | Martin Klein | Robert Ritter | James Richardson | David G Birch | Albert O Edwards | Wojciech Kedzierski
Molecular vision | 2007

Autosomal dominant Stargardt disease-3 (STGD3) is caused by mutations in elongase of very long chain fatty acids-4 (ELOVL4). The goal of this study was to generate and characterize heterozygous and homozygous knockin-mice that carry a human STGD3 pathogenic mutation in the mouse Elovl4 gene.

Pubmed ID: 17356513

Research resources used in this publication

None found

Additional research tools detected in this publication

Antibodies used in this publication

None found

Associated grants

  • Agency: NEI NIH HHS, United States
    Id: R01 EY014467
  • Agency: NEI NIH HHS, United States
    Id: EY 05235
  • Agency: NEI NIH HHS, United States
    Id: EY014467
  • Agency: NEI NIH HHS, United States
    Id: EY15409
  • Agency: NEI NIH HHS, United States
    Id: R01 EY005235
  • Agency: NEI NIH HHS, United States
    Id: R03 EY015409

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129/SvEv (tool)

RRID:MGI:5653381

laboratory mouse with name 129/SvEv from MGI.

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