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Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies.
Arimura, Takuro; Helbling-Leclerc, Anne; Massart, Catherine; Varnous, Shaida; Niel, Florence; Lacène, Emmanuelle; Fromes, Yves; Toussaint, Marcel; Mura, Anne-Marie; Keller, Dagmar I; Amthor, Helge; Isnard, Richard; Malissen, Marie; Schwartz, Ketty; Bonne, Gisèle.
Affiliation
  • Arimura T; Inserm UR582, Institut de Myologie, GH Pitié-Salpêtrière, Paris, France.
Hum Mol Genet ; 14(1): 155-69, 2005 Jan 01.
Article in En | MEDLINE | ID: mdl-15548545
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Collection: 01-internacional Database: MEDLINE Main subject: Cardiomyopathy, Dilated / Mutation, Missense / Muscular Dystrophy, Emery-Dreifuss / Lamin Type A / Disease Models, Animal / Muscular Dystrophy, Animal Limits: Animals / Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2005 Document type: Article Affiliation country: France Country of publication: United kingdom
Search on Google
Add to My VHL
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Cardiomyopathy, Dilated / Mutation, Missense / Muscular Dystrophy, Emery-Dreifuss / Lamin Type A / Disease Models, Animal / Muscular Dystrophy, Animal Limits: Animals / Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2005 Document type: Article Affiliation country: France Country of publication: United kingdom