Disruption of the Basal Body Protein POC1B Results in Autosomal-Recessive Cone-Rod Dystrophy

Exome sequencing revealed a homozygous missense mutation (c.317C>G [p.Arg106Pro]) in POC1B, encoding POC1 centriolar protein B, in three siblings with autosomal-recessive cone dystrophy or cone-rod dystrophy and compound-heterozygous POC1B mutations (c.199_201del [p.Gln67del] and c.810+1G>T) i...

Descripción completa

Detalles Bibliográficos
Autores principales: Roosing, Susanne, Lamers, Ideke J.C., de Vrieze, Erik, van den Born, L. Ingeborgh, Lambertus, Stanley, Arts, Heleen H., Peters, Theo A., Hoyng, Carel B., Kremer, Hannie, Hetterschijt, Lisette, Letteboer, Stef J.F., van Wijk, Erwin, Roepman, Ronald, den Hollander, Anneke I., Cremers, Frans P.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4129401/
https://www.ncbi.nlm.nih.gov/pubmed/25018096
http://dx.doi.org/10.1016/j.ajhg.2014.06.012

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4129401/
https://www.ncbi.nlm.nih.gov/pubmed/25018096
http://dx.doi.org/10.1016/j.ajhg.2014.06.012

Ejemplares similares