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Volumn 18, Issue 2, 1996, Pages 131-134

Merosin-negative non-Fukuyama-type congenital muscular dystrophy: A case report

Author keywords

Computed tomography; Congenital muscular dystrophy; Magnetic resonance imaging; Merosin; Non Fukuyama type

Indexed keywords

CREATINE KINASE; MEROSIN;

EID: 0029921882     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/0387-7604(95)00140-9     Document Type: Article
Times cited : (4)

References (12)
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  • 4
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    • Clinical phenotype in congenital muscular dystrophy: Correlation with expression of merosin in skeletal muscle
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    • (1995) Neuromusc Disord , vol.5 , pp. 301-305
    • Philpot, J.1    Sewry, C.2    Pennock, J.3
  • 6
    • 0028066764 scopus 로고
    • Human laminin M chain (merosin): Complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues
    • Vuolteenaho R, Nissinen M, Sainio K, et al. Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues. J Cell Biol 1994; 124: 381-94.
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    • Vuolteenaho, R.1    Nissinen, M.2    Sainio, K.3
  • 7
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    • Congenital muscular dystrophy of non-Fukuyama type with characteristic CT images
    • Yoshioka M, Kuroki S, Mizue H. Congenital muscular dystrophy of non-Fukuyama type with characteristic CT images. Brain Dev (Tokyo) 1987; 9: 316-8.
    • (1987) Brain Dev (Tokyo) , vol.9 , pp. 316-318
    • Yoshioka, M.1    Kuroki, S.2    Mizue, H.3
  • 9
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    • Congenital muscular dystrophy (Fukuyama type). Repeated CT studies in 19 children
    • Yoshioka M, Okuno T, Ito M, et al. Congenital muscular dystrophy (Fukuyama type). Repeated CT studies in 19 children. Comput Tomogr 1981; 5: 81-8.
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  • 10
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    • Abnormal localization of laminin subunits in muscular dystrophies
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    • Localization of gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.