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Volumn 50, Issue 3, 2000, Pages 171-174

Analysis of the SMN and NAIP genes in Slovak spinal muscular atrophy patients

Author keywords

Hybrid SMN gene; NAIP gene; SMN gene; Spinal muscular atrophy

Indexed keywords

INHIBITOR OF APOPTOSIS PROTEIN; NERVE PROTEIN;

EID: 0033970091     PISSN: 00015652     EISSN: None     Source Type: Journal    
DOI: 10.1159/000022909     Document Type: Article
Times cited : (7)

References (12)
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    • Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy: New insights into molecular mechanisms for the disease
    • Hahnen E, Schonling J, Rudnik-Schoneborn S, Zarres K, Wirth B: Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy: New insights into molecular mechanisms for the disease. Am J Hum Genet 1996;59:1057-1065.
    • (1996) Am J Hum Genet , vol.59 , pp. 1057-1065
    • Hahnen, E.1    Schonling, J.2    Rudnik-Schoneborn, S.3    Zarres, K.4    Wirth, B.5
  • 3
    • 0030818315 scopus 로고    scopus 로고
    • Genomie variation and gene conversion in spinal muscular atrophy: Implications for disease process and clinical phenotype
    • Campbell I, Potter A, Ignatius J, Dubowitz V, Davies K: Genomie variation and gene conversion in spinal muscular atrophy: Implications for disease process and clinical phenotype. Am J Hum Genet 1997;61:40-50.
    • (1997) Am J Hum Genet , vol.61 , pp. 40-50
    • Campbell, I.1    Potter, A.2    Ignatius, J.3    Dubowitz, V.4    Davies, K.5
  • 5
    • 16744367337 scopus 로고
    • Incidence of spinal muscular atrophy and Duchenne muscular dystrophy in child population of middle Slovakia (in Slovak)
    • Kvasnicová M, Styková J, Hudec P: Incidence of spinal muscular atrophy and Duchenne muscular dystrophy in child population of middle Slovakia (in Slovak). Bratisl Lek Listy 1994; 95:78-82.
    • (1994) Bratisl Lek Listy , vol.95 , pp. 78-82
    • Kvasnicová, M.1    Styková, J.2    Hudec, P.3
  • 6
    • 0027057672 scopus 로고
    • Meeting report: International SMA Consortium Meeting
    • Munsat TM, Davies KE: Meeting report: International SMA Consortium Meeting. Neuromusc Disord 1992;2:423-428.
    • (1992) Neuromusc Disord , vol.2 , pp. 423-428
    • Munsat, T.M.1    Davies, K.E.2
  • 8
    • 0028785098 scopus 로고
    • Molecular analysis of candidate genes on chromosome 5ql3 in autosomal recessive spinal muscular atrophy: Evidence of homozygous deletions of SMN gene in unaffected individuals
    • Hahnen E, Forker R, Marke C, Rudnik-Schoncborn S, Schonling J, Zerres K, Wirth B: Molecular analysis of candidate genes on chromosome 5ql3 in autosomal recessive spinal muscular atrophy: Evidence of homozygous deletions of SMN gene in unaffected individuals. Hum Mol Genet 1995;4:1927-1933.
    • (1995) Hum Mol Genet , vol.4 , pp. 1927-1933
    • Hahnen, E.1    Forker, R.2    Marke, C.3    Rudnik-Schoncborn, S.4    Schonling, J.5    Zerres, K.6    Wirth, B.7
  • 9
    • 0029117950 scopus 로고
    • Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: Association of marker gentoype with disease severity and candidate cDNAs
    • Wirth B, Hahnen E, Morgan K, DiDonato CJ, Dadze A, Rudnik-Schoneborn S, Simard LR, Zerres K, Burghes AHM: Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: Association of marker gentoype with disease severity and candidate cDNAs. Hum Mol Genet 1995;4:1273-1284.
    • (1995) Hum Mol Genet , vol.4 , pp. 1273-1284
    • Wirth, B.1    Hahnen, E.2    Morgan, K.3    DiDonato, C.J.4    Dadze, A.5    Rudnik-Schoneborn, S.6    Simard, L.R.7    Zerres, K.8    Burghes, A.H.M.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.