Identification of a Novel Gene on 10q22.1 Causing Autosomal Dominant Retinitis Pigmentosa (adRP)

Whole-genome linkage mapping identified a region on chromosome 10q21.3–q22.1 with a maximum LOD score of 3.0 at 0 % recombination in a six-generation family with autosomal dominant retinitis pigmentosa (adRP). All known adRP genes and X-linked RP genes were excluded in the family by a combination of...

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Publicado en:Adv Exp Med Biol
Main Authors: Daiger, Stephen P., Sullivan, Lori S., Bowne, Sara J., Koboldt, Daniel C., Blanton, Susan H., Wheaton, Dianna K., Avery, Cheryl E., Cadena, Elizabeth D., Koenekoop, Robert K., Fulton, Robert S., Wilson, Richard K., Weinstock, George M., Lewis, Richard A., Birch, David G.
Formato: Artigo
Idioma:Inglês
Publicado: 2016
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4906966/
https://ncbi.nlm.nih.gov/pubmed/26427411
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-3-319-17121-0_26
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