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Volumn 57, Issue 3, 2009, Pages 242-251
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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
a
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Author keywords
[No Author keywords available]
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Indexed keywords
NOTCH RECEPTOR;
NOTCH3 PROTEIN, HUMAN;
BRAIN;
CADASIL;
DIAGNOSTIC PROCEDURE;
EXON;
GENE DELETION;
GENETICS;
HUMAN;
NUCLEAR MAGNETIC RESONANCE IMAGING;
PATHOLOGY;
POINT MUTATION;
PROGNOSIS;
REVIEW;
SKIN;
VASCULAR SMOOTH MUSCLE;
VASCULARIZATION;
BRAIN;
CADASIL;
EXONS;
GENE DELETION;
HUMANS;
MAGNETIC RESONANCE IMAGING;
MOLECULAR DIAGNOSTIC TECHNIQUES;
MUSCLE, SMOOTH, VASCULAR;
POINT MUTATION;
PROGNOSIS;
RECEPTORS, NOTCH;
SKIN;
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EID: 67649209033
PISSN: 00471860
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
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Times cited : (4)
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References (37)
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