Identification and population history of CYP4V2 mutations in patients with Bietti crystalline corneoretinal dystrophy

To identify known and novel CYP4V2 mutations in patients with Bietti crystalline cornea (BCD), expand the spectrum of CYP4V2 mutations, and characterize the population history of the c.802-8_810del17insGC mutation common in Asian populations, genomic DNA was isolated from peripheral blood samples fr...

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Publicado en:Eur J Hum Genet
Autores principales: Jiao, Xiaodong, Li, Anren, Jin, Zi-Bing, Wang, Xinjing, Iannaccone, Alessandro, Traboulsi, Elias I, Gorin, Michael B, Simonelli, Francesca, Hejtmancik, J Fielding
Formato: Artigo
Lenguaje:Inglês
Publicado: Nature Publishing Group 2017
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5386409/
https://ncbi.nlm.nih.gov/pubmed/28051075
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2016.184
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