A novel mutation (C67Y)in the NOTCH3 gene in a Korean CADASIL patient.
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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in a Chinese pedigree: A case report using brain magnetic resonance imaging and biospyDetection of the founder effect in Finnish CADASIL families.Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: Phenotypic and mutational spectrum in patients from mainland China.
P2860
A novel mutation (C67Y)in the NOTCH3 gene in a Korean CADASIL patient.
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2003 nî lūn-bûn
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2003 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի փետրվարին հրատարակված գիտական հոդված
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2003年の論文
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2003年論文
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2003年論文
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2003年論文
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2003年論文
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2003年論文
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2003年论文
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name
A novel mutation (C67Y)in the NOTCH3 gene in a Korean CADASIL patient.
@ast
A novel mutation (C67Y)in the NOTCH3 gene in a Korean CADASIL patient.
@en
type
label
A novel mutation (C67Y)in the NOTCH3 gene in a Korean CADASIL patient.
@ast
A novel mutation (C67Y)in the NOTCH3 gene in a Korean CADASIL patient.
@en
prefLabel
A novel mutation (C67Y)in the NOTCH3 gene in a Korean CADASIL patient.
@ast
A novel mutation (C67Y)in the NOTCH3 gene in a Korean CADASIL patient.
@en
P2093
P1476
A novel mutation (C67Y)in the NOTCH3 gene in a Korean CADASIL patient.
@en
P2093
Chang-Seok Ki
Hahn-Young Kim
Jae-Chul Kwon
Jong-Won Kim
Jung-Im Seok
So-Young Moon
Yeon-Lim Suh
P304
P356
10.3346/JKMS.2003.18.1.141
P577
2003-02-01T00:00:00Z