CDHR1 mutations in retinal dystrophies

We report ophthalmic and genetic findings in patients with autosomal recessive retinitis pigmentosa (RP), cone-rod dystrophy (CRD) or cone dystrophy (CD) harboring potential pathogenic variants in the CDHR1 gene. Detailed ophthalmic examination was performed in seven sporadic and six familial subjec...

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Detalles Bibliográficos
Autores principales: Stingl, Katarina, Mayer, Anja K., Llavona, Pablo, Mulahasanovic, Lejla, Rudolph, Günther, Jacobson, Samuel G., Zrenner, Eberhart, Kohl, Susanne, Wissinger, Bernd, Weisschuh, Nicole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539332/
https://www.ncbi.nlm.nih.gov/pubmed/28765526
http://dx.doi.org/10.1038/s41598-017-07117-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539332/
https://www.ncbi.nlm.nih.gov/pubmed/28765526
http://dx.doi.org/10.1038/s41598-017-07117-8

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