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Volumn 21, Issue 3, 2001, Pages 202-206

Prenatal diagnosis of hereditary spastic paraplegia

Author keywords

Paraplegia; Spasticity; Strumpell Lorrain

Indexed keywords

MICROSATELLITE DNA;

EID: 0035056728     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/1097-0223(200103)21:3<202::AID-PD4>3.0.CO;2-U     Document Type: Article
Times cited : (7)

References (20)
  • 2
    • 0032511186 scopus 로고    scopus 로고
    • Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease
    • (1998) Cell , vol.93 , pp. 973-983
    • Casari, G.1    Fusco, M.2    Ciarmatori, S.3
  • 6
  • 9
    • 0028872909 scopus 로고
    • Autosomal dominant familial spastic paraplegia: Reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity
    • (1995) Am J Hum Genet , vol.56 , pp. 183-187
    • Gispert, S.1    Santos, N.2    Damen, R.3
  • 20
    • 0033069503 scopus 로고    scopus 로고
    • Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy
    • (1999) Am J Hum Genet , vol.64 , pp. 586-593
    • Seri, M.1    Cusano, R.2    Forabosco, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.