about
Molecular Characterization of FZD4, LRP5, and TSPAN12 in Familial Exudative Vitreoretinopathy.Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis.Leber's hereditary optic neuropathy mutations in ethambutol-induced optic neuropathy.Growth kinetics and transplantation of human retinal progenitor cells.Prediction of rebound phenomenon after removal of hemiepiphyseal staples in patients with idiopathic genu valgum deformity.MtDNA m.3472T>C could be classified as a primary mutation of Leber's hereditary optic neuropathy.Mitochondrial DNA content is decreased in autosomal dominant optic atrophy.Novel MT-ND5 gene mutation identified in Leber's hereditary optic neuropathy patient using mitochondrial genome sequencing.Diagnostic application of an extensive gene panel for Leber congenital amaurosis with severe genetic heterogeneity.Mutation spectrum of RB1 gene in Korean bilateral retinoblastoma patients using direct sequencing and gene dosage analysis.Spectrum of the mitochondrial DNA mutations of Leber's hereditary optic neuropathy in Koreans.Ophthalmoplegia diagnosis.
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description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Ji Yeon Kim
@en
Ji Yeon Kim
@es
Ji Yeon Kim
@sl
type
label
Ji Yeon Kim
@en
Ji Yeon Kim
@es
Ji Yeon Kim
@sl
prefLabel
Ji Yeon Kim
@en
Ji Yeon Kim
@es
Ji Yeon Kim
@sl
P106
P31
P496
0000-0003-2147-6326