The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease

Author:

Davignon Laurianne,Chauveau Claire,Julien Cédric,Dill Corinne,Duband-Goulet Isabelle,Cabet Eva,Buendia Brigitte,Lilienbaum Alain,Rendu John,Minot Marie Christine,Guichet Agnès,Allamand Valérie,Vadrot Nathalie,Fauré Julien,Odent Sylvie,Lazaro Leïla,Leroy Jean Paul,Marcorelles Pascale,Dubourg Odile,Ferreiro Ana

Funder

the Association Institut de Myologie

the Institut National de la Santé et la Recherche Médicale (Inserm)

the Université Pierre et Marie Curie and the Université Paris Diderot, France

the International Graduate Program for Muscle Sciences

GK1631 ‘Myograd’

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Reference61 articles.

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4. Multicore disease. A recently recognized congenital myopathy associated with multifocal degeneration of muscle fibres;Engel;Mayo. Clin. Proc.,1971

5. Multi-minicore disease-searching for boundaries: Phenotype analysis of 38 cases

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