Author:
Qi Yu-He,Gao Feng-Juan,Hu Fang-Yuan,Zhang Sheng-Hai,Chen Jun-Yi,Huang Wan-Jing,Tian Guo-Hong,Wang Min,Gan De-Kang,Wu Ji-Hong,Xu Ge-Zhi
Funder
National Natural Science Foundation of China
Subject
Genetics(clinical),Genetics,Molecular Medicine
Reference44 articles.
1. Clinical and genetic characteristics of Korean occult macular dystrophy patients.;Ahn;Invest. Ophthalmol. Vis. Sci.,2013
2. Dominant mutations in RP1L1 are responsible for occult macular dystrophy.;Akahori;Am. J. Hum. Genet.,2010
3. The precision medicine initiative: a new national effort.;Ashley;JAMA,2015
4. Precision medicine initiative aims for a new generation of diagnostics and treatments: but is the promise of genetic targeting overinflated?;Barlas;P T,2015
5. Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene.;Bowne;Mol. Vis.,2003
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