p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small-vessel occlusion in elderly Japanese males.
about
Familial hypertrophic obstructive cardiomyopathy with the GLA E66Q mutation and zebra body.The Large Phenotypic Spectrum of Fabry Disease Requires Graduated Diagnosis and Personalized Therapy: A Meta-Analysis Can Help to Differentiate Missense MutationsAetiological diagnosis of middle-aged and elderly cryptogenic ischaemic cerebral vascular disease.Screening for Fabry's disease in young patients with ischemic stroke in a Chinese population.GLA mutation as a risk factor for later life small vessel ischaemic disease.Role of the p.E66Q variant of GLA in the progression of chronic kidney disease.Prevalence of Fabry disease and GLA c.196G>C variant in Japanese stroke patients.
P2860
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P2860
p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small-vessel occlusion in elderly Japanese males.
description
2013 nî lūn-bûn
@nan
2013年の論文
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年學術文章
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name
p.E66Q mutation in the GLA gen ...... ion in elderly Japanese males.
@en
p.E66Q mutation in the GLA gen ...... ion in elderly Japanese males.
@nl
type
label
p.E66Q mutation in the GLA gen ...... ion in elderly Japanese males.
@en
p.E66Q mutation in the GLA gen ...... ion in elderly Japanese males.
@nl
prefLabel
p.E66Q mutation in the GLA gen ...... ion in elderly Japanese males.
@en
p.E66Q mutation in the GLA gen ...... ion in elderly Japanese males.
@nl
P2093
P2860
P356
P1476
p.E66Q mutation in the GLA gen ...... ion in elderly Japanese males.
@en
P2093
K Nagamatsu
K Nakamura
Y Fukushima
Y Sekijima
P2860
P356
10.1111/ENE.12214
P577
2013-05-31T00:00:00Z