Associated Papers
Whole exome sequencing analysis identifies novel Stargardt disease-related gene mutations in Chinese Stargardt disease and retinitis pigmentosa patients.
Ng TK et al.
Eye (london, England), 2022
NOTCH3 mutations and clinical features in 33 mainland Chinese families with CADASIL.
Wang Z et al.
Journal of Neurology, Neurosurgery, and Psychiatry, 2011
Select a paper to view details