Associated Papers
Clinical presentations of X-linked retinoschisis in Taiwanese patients confirmed with genetic sequencing.
Wang NK et al.
Molecular Vision, 2015
Whole Exome Sequencing Reveals DYSF, FKTN, and ISPD Mutations in Congenital Muscular Dystrophy Without Brain or Eye Involvement.
Ceyhan-Birsoy O et al.
Journal of Neuromuscular Diseases, 0
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