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
A de novo paradigm for male infertility.
Oud MS et al.
Nature Communications, 2022
35013161 (PubMed )
Supplement: 41467_2021_27132_MOESM4_ESM.xlsx › Supplementary_Data_1
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