Associated Papers
Identification of 11 potentially relevant gene mutations involved in growth retardation, intellectual disability, joint contracture, and hepatopathy.
Diao H et al.
Medicine, 2018
30431579 (PubMed )
Supplement: medi-97-e13117-s001.xlsx › Sheet1
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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