Concepedia

Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin α2 chain gene

Sylvie Besse, Valérie Allamand, Jean‐Thomas Vilquin, Zhenlin Li, Christophe Poirier, Nicolas Vignier, Hisae Hori, Jean‐Louis Guénet, Pascale Guicheney

Neuromuscular Disorders · 2003 · 23 citations · 36 references

DOI

Concepts

References

36

A general method for isolation of high molecular weight DNA from eukaryotes

Nikolaus Blin, Darrel W. Stafford · Nucleic Acids Research · 1976 · 2.8K citations · Full text

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Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man

Haig H. Kazazian, Corinne Wong, Hagop Youssoufian et al. · Nature · 1988 · 928 citations

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A comprehensive genetic map of the mouse genome

William F. Dietrich, Joyce Miller, Robert Steen et al. · Nature · 1996 · 835 citations

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A new nomenclature for the laminins

Robert E. Burgeson, Matthias Chiquet, Rainer Deutzmann et al. · Matrix Biology · 1994 · 756 citations

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Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy

A. Leclerc, Xu Zhang, Haluk Topaloğlu et al. · Nature Genetics · 1995 · 628 citations

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