Carregant...

Lack of MEF2A mutations in coronary artery disease

Mutations in MEF2A have been implicated in an autosomal dominant form of coronary artery disease (adCAD1). In this study we sought to determine whether severe mutations in MEF2A might also explain sporadic cases of coronary artery disease (CAD). To do this, we resequenced the coding sequence and spl...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Weng, Li, Kavaslar, Nihan, Ustaszewska, Anna, Doelle, Heather, Schackwitz, Wendy, Hébert, Sybil, Cohen, Jonathan C., McPherson, Ruth, Pennacchio, Len A.
Format: Artigo
Idioma:Inglês
Publicat: American Society for Clinical Investigation 2005
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1070426/
https://ncbi.nlm.nih.gov/pubmed/15841183
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI200524186
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!