Common MFRP sequence variants are not associated with moderate to high hyperopia, isolated microphthalmia, and high myopia

PURPOSE: The membrane-type frizzled-related protein (MFRP) gene is selectively expressed in the retinal pigment epithelium and ciliary body, and mutations of this gene cause nanophthalmos. The MFRP gene may not be essential for retinal function but has been hypothesized to play a role in ocular axia...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Metlapally, Ravikanth, Li, Yi-Ju, Tran-Viet, Khanh-Nhat, Bulusu, Anuradha, White, Tristan R., Ellis, Jaclyn, Kao, Daniel, Young, Terri L.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Molecular Vision 2008
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2268852/
https://ncbi.nlm.nih.gov/pubmed/18334955
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