Associated Papers
Widespread RNA editing dysregulation in brains from autistic individuals.
Tran SS et al.
Nature Neuroscience, 2019
30559470 (PubMed )
Supplement: NIHMS1512053-supplement-Sup_Table_2.xlsx › 2b
A novel splice donor site mutation in EPHA2 caused congenital cataract in a Chinese family.
Bu J et al.
Indian Journal of Ophthalmology, 2016
27380975 (PubMed )
Supplement: IJO-64-364_Suppl2.pdf
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