The Loss of Vacuolar Protein Sorting 11 (vps11) Causes Retinal Pathogenesis in a Vertebrate Model of Syndromic Albinism | Zendy

Jennifer L. Thomas | Zendy; Thomas S. Vihtelic | Zendy; Aaron D. denDekker | Zendy; Gregory B. Willer | Zendy; Xixia Luo | Zendy; Taylor R. Murphy | Zendy; Ronald G. Gregg | Zendy; David R. Hyde | Zendy; Ryan Thummel | Zendy

Open Access

The Loss of Vacuolar Protein Sorting 11 (vps11) Causes Retinal Pathogenesis in a Vertebrate Model of Syndromic Albinism

Author(s) -

Jennifer L. Thomas,

Thomas S. Vihtelic,

Aaron D. denDekker,

Gregory B. Willer,

Xixia Luo,

Taylor R. Murphy,

Ronald G. Gregg,

David R. Hyde,

Ryan Thummel

Publication year - 2011

Publication title -

investigative ophthalmology and visual science

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.935

H-Index - 218

eISSN - 1552-5783

pISSN - 0146-0404

DOI - 10.1167/iovs.10-5957

Subject(s) - zebrafish , biology , melanosome , retinal pigment epithelium , retinal , retina , microbiology and biotechnology , genetics , mutant , gene , melanin , neuroscience , biochemistry

To establish the zebrafish platinum mutant as a model for studying vision defects caused by syndromic albinism diseases such as Chediak-Higashi syndrome, Griscelli syndrome, and Hermansky-Pudlak syndrome (HPS).

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