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Volumn 49, Issue 4, 2014, Pages 616-617

LAMA2 mutations in adult-onset muscular dystrophy with leukoencephalopathy

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA DYSTROGLYCAN; ALPHA7 INTEGRIN; ALPHA7BETA1 INTEGRIN; LAMININ ALPHA2; UNCLASSIFIED DRUG;

EID: 84896109592     PISSN: 0148639X     EISSN: 10974598     Source Type: Journal    
DOI: 10.1002/mus.24147     Document Type: Article
Times cited : (4)

References (7)
  • 2
    • 0000122091 scopus 로고
    • Congenital muscular dystrophy
    • Engel AG, Banker BQ, editors. New York: McGraw-Hill;
    • Banker BQ. Congenital muscular dystrophy. In: Engel AG, Banker BQ, editors. Myology. Vol. 2. New York: McGraw-Hill; 1986. p 1367-1382.
    • (1986) Myology , vol.2 , pp. 1367-1382
    • Banker, B.Q.1
  • 4
    • 77950960625 scopus 로고    scopus 로고
    • Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations
    • Geranmayeh F, Clement E, Feng LH, Sewry C, Pagan J, Mein R, et al. Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations. Neuromuscul Disord 2010;20:241-250.
    • (2010) Neuromuscul Disord , vol.20 , pp. 241-250
    • Geranmayeh, F.1    Clement, E.2    Feng, L.H.3    Sewry, C.4    Pagan, J.5    Mein, R.6
  • 6
    • 18844466352 scopus 로고    scopus 로고
    • Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study
    • He Y, Jones KJ, Vignier N, Morgan G, Chevallay M, Barois A, et al. Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study. Neurology 2001;57:1319-1322.
    • (2001) Neurology , vol.57 , pp. 1319-1322
    • He, Y.1    Jones, K.J.2    Vignier, N.3    Morgan, G.4    Chevallay, M.5    Barois, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.