Congenital muscular dystrophy with merosin deficiency.

No abstract is available for this paper.

• Publication year

  1994

• Venue

  Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie

• Publication date

  1994-04-01

• Fields of study

  Medicine

• Identifiers
  PMID 8000914
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus.

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  1993cited by this paper
• The laminin family.

  1993cited by this paper
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  1992cited by this paper
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  1992cited by this paper
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  1991cited by this paper
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  1991cited by this paper
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  1990cited by this paper
• Association of dystrophin and an integral membrane glycoprotein

  1989cited by this paper
• Merosin, a protein specific for basement membranes of Schwann cells, striated muscle, and trophoblast, is expressed late in nerve and muscle development.

  1988cited by this paper
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  1986cited by this paper
• Fibronectin, laminin, type I, III and IV collagens in Duchenne's muscular dystrophy, congenital muscular dystrophies and congenital myopathies: an immunocytochemical study.

  1985cited by this paper
• Collagen types in neuromuscular diseases.

  1982cited by this paper
• A role for collagen in the pathogenesis of muscular dystrophy?

  1980cited by this paper

• LAMA2 variants associated with muscular dystrophy, brain structural abnormalities, and epilepsy: a genotype-phenotype study

  2026cites this paper
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• [Michel Fardeau, a life dedicated to myology and its innovations].

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• Dual AAV gene therapy using laminin-linking proteins ameliorates muscle and nerve defects in LAMA2-related muscular dystrophy

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  2017cites this paper
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• Laminin-211 in skeletal muscle function

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• [Congenital muscular dystrophies in children].

  2013cites this paper
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  2012cites this paper
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  2012cites this paper
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