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Volumn 51, Issue 6, 2002, Pages 681-685

Novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q33-q34

Author keywords

[No Author keywords available]

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;

EID: 0036260783     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.10204     Document Type: Article
Times cited : (40)

References (19)
  • 4
    • 0027363223 scopus 로고
    • Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q
    • (1993) Nat Genet , vol.5 , pp. 163-167
    • Hazan, J.1    Lamy, C.2    Melki, J.3
  • 15
    • 0029945706 scopus 로고    scopus 로고
    • Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
    • (1996) Am J Hum Genet , vol.58 , pp. 1323-1337
    • Sobel, E.1    Lange, K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.