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Blood Transcriptome Profiling in Myasthenia Gravis Patients to Assess Disease Activity: A Pilot RNA-seq Study
Experimental Neurobiology, 2016
29 2017-07-25 -
KIF11 mutations are a common cause of autosomal dominant familial exudative vitreoretinopathy
British Journal of Ophthalmology, 2015
43 2017-07-25 -
NTRK1 fusions for the therapeutic intervention of Korean patients with colon cancer
Oncotarget, 2015
31 2016-01-19 -
Unique Variants in OPN1LW Cause Both Syndromic and Nonsyndromic X-Linked High Myopia Mapped to MYP1
Investigative OphthaImology &Visual Science, 2015
35 2015-10-14
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