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Volumn 98, Issue 5, 1996, Pages 524-527

Deletion analysis of the SMN and NAIP genes in Kuwaiti patients with spinal muscular atrophy

Author keywords

[No Author keywords available]

Indexed keywords

NERVE PROTEIN;

EID: 0029853107     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050253     Document Type: Article
Times cited : (23)

References (23)
  • 1
    • 0011802494 scopus 로고
    • Delineating the mutations in spinal muscular atrophy: Improved molecular detection and genotype-phenotype correlations
    • Aubry HL, MacKenzie AE, Surh LC (1995) Delineating the mutations in spinal muscular atrophy: improved molecular detection and genotype-phenotype correlations. Am J Hum Genet 57 Suppl:A234
    • (1995) Am J Hum Genet , vol.57 , Issue.SUPPL.
    • Aubry, H.L.1    MacKenzie, A.E.2    Surh, L.C.3
  • 3
    • 0028978717 scopus 로고
    • Genetic homogeneity between childhood-onset and adult-onset autosomal recessive spinal muscular atrophy
    • Brahe C, Servidei S, Zappata S, Ricci E, Tonali P, Neri G (1995b) Genetic homogeneity between childhood-onset and adult-onset autosomal recessive spinal muscular atrophy. Lancet 346:741-742
    • (1995) Lancet , vol.346 , pp. 741-742
    • Brahe, C.1    Servidei, S.2    Zappata, S.3    Ricci, E.4    Tonali, P.5    Neri, G.6
  • 5
    • 0343381790 scopus 로고
    • Extended haplotype analysis and deletions in the SMN gene in Polish families with spinal muscular atrophy
    • Brzustowicz LM, Ricketts A, Hausmanowa-Petrusewicz I (1995) Extended haplotype analysis and deletions in the SMN gene in Polish families with spinal muscular atrophy. Am J Hum Genet 57 Suppl:A209
    • (1995) Am J Hum Genet , vol.57 , Issue.SUPPL.
    • Brzustowicz, L.M.1    Ricketts, A.2    Hausmanowa-Petrusewicz, I.3
  • 11
    • 0342512186 scopus 로고
    • Sensitivity of direct testing for SMN gene deletions in autosomal spinal muscular atrophy
    • Kant JA, Rennert H, Joshi I, Wilson RB (1995) Sensitivity of direct testing for SMN gene deletions in autosomal spinal muscular atrophy. Am J Hum Genet 57 Suppl:A331
    • (1995) Am J Hum Genet , vol.57 , Issue.SUPPL.
    • Kant, J.A.1    Rennert, H.2    Joshi, I.3    Wilson, R.B.4
  • 16
    • 44949282843 scopus 로고
    • Workshop report: International SMA consortium meeting
    • Munsat TL (1991) Workshop report: international SMA consortium meeting. Neuromuscul Disord 1:81
    • (1991) Neuromuscul Disord , vol.1 , pp. 81
    • Munsat, T.L.1
  • 23
    • 33847473099 scopus 로고
    • Molecular analysis of candidate genes on 5q13 in autosomal recessive spinal muscular atrophy: Evidence of homozygous deletions of the SMN gene in unaffected individuals
    • Wirth B, Hahnen E, Forkert R, Marke C, Rudnik-Schoneborn S, Zerres K (1995) Molecular analysis of candidate genes on 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals. Am J Hum Genet 57 Suppl:A23
    • (1995) Am J Hum Genet , vol.57 , Issue.SUPPL.
    • Wirth, B.1    Hahnen, E.2    Forkert, R.3    Marke, C.4    Rudnik-Schoneborn, S.5    Zerres, K.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.