CADASIL syndrome in a large Turkish kindred caused by the R90C mutation in the Notch3 receptor.
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Neurogenomics in Africa: Perspectives, progress, possibilities and prioritiesCerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy syndrome mutations increase susceptibility to spreading depression.CADASIL in Arabs: clinical and genetic findings.Vascular cognitive impairment: Modeling a critical neurologic disease in vitro and in vivo.Genetic animal models of cerebral vasculopathies.CADASIL and migraine: A narrative review.Neoplastic lesions in CADASIL syndrome: report of an autopsied Japanese case.R141C Mutation of NOTCH3 Gene in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.Regional volume analysis of the Parkinson disease brain in early disease stage: gray matter, white matter, striatum, and thalamus.CADASIL: MRI may be normal in the fourth decade of life - a case report.
P2860
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P2860
CADASIL syndrome in a large Turkish kindred caused by the R90C mutation in the Notch3 receptor.
description
2002 nî lūn-bûn
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2002年の論文
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2002年学术文章
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2002年学术文章
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2002年学术文章
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name
CADASIL syndrome in a large Tu ...... tation in the Notch3 receptor.
@en
CADASIL syndrome in a large Tu ...... tation in the Notch3 receptor.
@nl
type
label
CADASIL syndrome in a large Tu ...... tation in the Notch3 receptor.
@en
CADASIL syndrome in a large Tu ...... tation in the Notch3 receptor.
@nl
prefLabel
CADASIL syndrome in a large Tu ...... tation in the Notch3 receptor.
@en
CADASIL syndrome in a large Tu ...... tation in the Notch3 receptor.
@nl
P2093
P2860
P1476
CADASIL syndrome in a large Tu ...... tation in the Notch3 receptor.
@en
P2093
P2860
P356
10.1046/J.1468-1331.2002.00344.X
P577
2002-01-01T00:00:00Z