A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree

Detalles Bibliográficos
Autores principales: Cheng, Jingliang, Fu, Jiewen, Zhou, Qi, Xiang, Xiaohong, Wei, Chunli, Yang, Lisha, Fu, Shangyi, Khan, Md. Asaduzzaman, Lv, Hongbin, Fu, Junjiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Short Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6484291/
https://www.ncbi.nlm.nih.gov/pubmed/30892800
http://dx.doi.org/10.1111/jcmm.14278

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6484291/
https://www.ncbi.nlm.nih.gov/pubmed/30892800
http://dx.doi.org/10.1111/jcmm.14278

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