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Volumn 116, Issue 3, 2005, Pages 242-
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Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
a
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Author keywords
[No Author keywords available]
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Indexed keywords
CELL SURFACE RECEPTOR;
NOTCH RECEPTOR;
NOTCH3 PROTEIN, HUMAN;
ONCOPROTEIN;
ARTICLE;
BRAIN INFARCTION;
CEREBRAL ARTERY DISEASE;
DOMINANT GENE;
GENETICS;
HUMAN;
MISSENSE MUTATION;
MULTIINFARCT DEMENTIA;
STOP CODON;
CEREBRAL ARTERIAL DISEASES;
CEREBRAL INFARCTION;
CODON, NONSENSE;
DEMENTIA, VASCULAR;
GENES, DOMINANT;
HUMANS;
MUTATION, MISSENSE;
PROTO-ONCOGENE PROTEINS;
RECEPTORS, CELL SURFACE;
RECEPTORS, NOTCH;
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EID: 15944391673
PISSN: 03406717
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (1)
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References (0)
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