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Volumn 58, Issue 1, 1996, Pages 171-181
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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval
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Author keywords
[No Author keywords available]
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Indexed keywords
ADULT;
ARTICLE;
AUTOSOMAL DOMINANT DISORDER;
BRAIN INFARCTION;
CEREBROVASCULAR DISEASE;
CHROMOSOME 19P;
FAMILY STUDY;
GENE LOCUS;
GENE MAPPING;
GENETIC LINKAGE;
GENETIC MARKER;
GENETIC POLYMORPHISM;
GENOTYPE;
HEREDITARY ATAXIA;
HUMAN;
LEUKOENCEPHALOPATHY;
MAJOR CLINICAL STUDY;
MIGRAINE;
PEDIGREE;
PRIORITY JOURNAL;
ATAXIA;
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EID: 0029655609
PISSN: 00029297
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (68)
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References (5)
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