Identification and Subcellular Localization of the RP1 Protein in Human and Mouse Photoreceptors

PURPOSE: Mutations in the RP1gene account for 6% to 10% of autosomal dominant retinitis pigmentosa (adRP). Previous studies have shown that the RP1gene is expressed specifically in photoreceptor cells. So far, little is known about the RP1 protein or how mutations in RP1lead to photoreceptor cell de...

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Main Authors: Liu, Qin, Zhou, Jie, Daiger, Stephen P., Farber, Debora B., Heckenlively, John R., Smith, Julie E., Sullivan, Lori S., Zuo, Jian, Milam, Ann H., Pierce, Eric A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2002
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1963488/
https://ncbi.nlm.nih.gov/pubmed/11773008
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