Searching the Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

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

Publication data is provided by the National Library of Medicine ® and PubMed ®. Data is retrieved from PubMed ® on a weekly schedule. For terms and conditions see the National Library of Medicine Terms and Conditions.

This is a list of tools and resources that we have found mentioned in this publication.


129/SvEv (tool)

RRID:MGI:5653381

laboratory mouse with name 129/SvEv from MGI.

View all literature mentions