Multiethnic involvement in autosomal-dominant optic atrophy in Singapore

被引:0
作者
J L Loo
S Singhal
A V Rukmini
S Tow
P Amati-Bonneau
V Procaccio
D Bonneau
J J Gooley
P Reynier
M Ferré
D Milea
机构
[1] Singapore National Eye Centre,Department of Neuro
[2] Singapore Eye Research Institute,Ophthalmology
[3] Duke-NUS Graduate Medical School,Department of Biochemistry and Genetics
[4] UMR CNRS6214-INSERM1083,undefined
[5] University Hospital of Angers,undefined
来源
Eye | 2017年 / 31卷
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中图分类号
学科分类号
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页码:475 / 480
页数:5
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[21]  
Mayer S(2015)Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathy Ophthalmology 122 1777-1785
[22]  
Moore A(2001)Pupillary responses to high-irradiance blue light correlate with glaucoma severity Hum Mol Genet 10 1369-1378
[23]  
Chao de la Barca JM(2002)Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy Graefes Arch Clin Exp Ophthalmol 240 758-764
[24]  
Prunier-Mirebeau D(2006)Leber's hereditary optic neuropathy: clinical and molecular genetic results in a patient with a point mutation at np T11253C (isoleucine to threonine) in the Hum Genet 118 767-771
[25]  
Amati-Bonneau P(2015) gene and spontaneous recovery Front Neurol 6 5-324
[26]  
Ferré M(2010)Activation of cryptic splice sites is a frequent splicing defect mechanism caused by mutations in exon and intron sequences of the Clin Exp Ophthalmol 38 322-e236
[27]  
Sarzi E(2013) gene Brain 136 e236-121
[28]  
Bris C(2010)Dissociation of pupillary post-illumination responses from visual function in confirmed OPA1 c.983A >G and c.2708_2711delTTAG autosomal dominant optic atrophy Genome Res 20 110-362
[29]  
Ferré M(2011)Selective wavelength pupillometry in Leber hereditary optic neuropathy Mol Syst Biol 7 539-874
[30]  
Amati-Bonneau P(2014)Sensorineural hearing loss in OPA1-linked disorders Nat Methods 11 361-249