Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene

PURPOSE: To determine the full-length sequence of a gene with similarity to RP1 and to screen for mutations in this newly characterized gene, named retinitis pigmentosa 1-like 1(RP1L1). Since mutations in the RP1 gene cause autosomal dominant retinitis pigmentosa, it is possible that mutations in RP...

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Detalhes bibliográficos
Main Authors: Bowne, Sara J., Daiger, Stephen P., Malone, Kimberly A., Heckenlively, John R., Kennan, Avril, Humphries, Peter, Hughbanks-Wheaton, Dianna, Birch, David G., Liu, Qin, Pierce, Eric A., Zuo, Jian, Huang, Qian, Donovan, Danyel D., Sullivan, Lori S.
Formato: Artigo
Idioma:Inglês
Publicado em: 2003
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2580755/
https://ncbi.nlm.nih.gov/pubmed/12724644
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