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Volumn 51, Issue 6, 2002, Pages 681-685
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Novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q33-q34
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Author keywords
[No Author keywords available]
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Indexed keywords
ADULT;
AGED;
ARTICLE;
AUTOSOMAL DOMINANT DISORDER;
CHROMOSOME 12Q;
CHROMOSOME 14Q;
CHROMOSOME 15Q;
CHROMOSOME 19Q;
CHROMOSOME 2P;
CHROMOSOME 2Q;
CHROMOSOME 8P;
CHROMOSOME 9Q;
CHROMOSOME MAP;
CLINICAL ARTICLE;
DISABILITY;
FAMILY;
FEMALE;
GENE LOCUS;
GENETIC LINKAGE;
GENOME;
HAPLOTYPE;
HEREDITARY MOTOR SENSORY NEUROPATHY;
HUMAN;
ITALY;
MALE;
ONSET AGE;
PHENOTYPE;
PRIORITY JOURNAL;
SPASTICITY;
URGE INCONTINENCE;
URINE INCONTINENCE;
WHEELCHAIR;
ADOLESCENT;
ADULT;
AGED;
CHILD;
CHILD, PRESCHOOL;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 9;
FEMALE;
HAPLOTYPES;
HUMANS;
INFANT;
INFANT, NEWBORN;
ITALY;
LINKAGE (GENETICS);
MALE;
MIDDLE AGED;
PEDIGREE;
SPASTIC PARAPLEGIA, HEREDITARY;
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EID: 0036260783
PISSN: 03645134
EISSN: None
Source Type: Journal
DOI: 10.1002/ana.10204 Document Type: Article |
Times cited : (40)
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References (19)
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