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Volumn 133, Issue 1, 2010, Pages 7-8

Erratum: Copy number variants-an unexpected risk factor for the idiopathic generalized epilepsies (Brain (2010) 133 (7-8) DOI: 10.1093/brain/awp332);Copy number variants-an unexpected risk factor for the idiopathic generalized epilepsies

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL; MICROTUBULE ASSOCIATED PROTEIN 1;

EID: 74249086521     PISSN: 00068950     EISSN: 14602156     Source Type: Journal    
DOI: 10.1093/brain/awq016     Document Type: Erratum
Times cited : (20)

References (9)
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    • 0041343159 scopus 로고    scopus 로고
    • Association between genetic variation of CACNA1H and childhood absence epilepsy
    • Chen Y, Lu J, Pan H, Zhang Y, Wu H, Xu K, et al. Association between genetic variation of CACNA1H and childhood absence epilepsy. Ann Neurol 2003; 54: 239-43.
    • (2003) Ann Neurol , vol.54 , pp. 239-243
    • Chen, Y.1    Lu, J.2    Pan, H.3    Zhang, Y.4    Wu, H.5    Xu, K.6
  • 2
    • 74249093919 scopus 로고    scopus 로고
    • Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idio-pathic generalized epilepsies
    • Advance Access published on October 20, 2009
    • de Kovel CGF, Trucks H, Helbig I, Mefford HC, Baker C, Leu C, et al. Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idio-pathic generalized epilepsies. Brain 2009. Advance Access published on October 20, 2009.
    • (2009) Brain
    • De Kovel, C.G.F.1    Trucks, H.2    Helbig, I.3    Mefford, H.C.4    Baker, C.5    Leu, C.6
  • 3
    • 70350774172 scopus 로고    scopus 로고
    • Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: Precedent for disorders with complex inheritance
    • Dibbens LM, Mullen S, Helbig I, Mefford HC, Bayly MA, Bellows S, et al. Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance. Hum Mol Genet 2009; 18: 3626-3631
    • (2009) Hum Mol Genet , vol.18 , pp. 3626-3631
    • Dibbens, L.M.1    Mullen, S.2    Helbig, I.3    Mefford, H.C.4    Bayly, M.A.5    Bellows, S.6
  • 5
    • 68649123353 scopus 로고    scopus 로고
    • Duplication hotspots, rare genomic disorders, and common disease
    • Mefford HC, Eichler EE. Duplication hotspots, rare genomic disorders, and common disease. Curr Opin Genet Dev 2009; 19: 196-204.
    • (2009) Curr Opin Genet Dev , vol.19 , pp. 196-204
    • Mefford, H.C.1    Eichler, E.E.2
  • 6
    • 39749154724 scopus 로고    scopus 로고
    • A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures
    • Sharp AJ, Mefford HC, Li K, Baker C, Skinner C, Stevenson RE, et al. A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures. Nat Genet 2008; 40: 322-328
    • (2008) Nat Genet , vol.40 , pp. 322-328
    • Sharp, A.J.1    Mefford, H.C.2    Li, K.3    Baker, C.4    Skinner, C.5    Stevenson, R.E.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.