Miscues on the “lack of MEF2A mutations” in coronary artery disease

Ítems similars

• Mutation of MEF2A in an Inherited Disorder with Features of Coronary Artery Disease
  per: Wang, Lejin, et al.
  Publicat: (2003)
• Lack of MEF2A mutations in coronary artery disease
  per: Weng, Li, et al.
  Publicat: (2005)
• Transcription factor MEF2A mutations in patients with coronary artery disease
  per: Bhagavatula, M.R. Krishna, et al.
  Publicat: (2004)
• Lack of Association between the MEF2A Gene and Coronary Artery Disease in Iranian Families
  per: Inanloo Rahatloo, Kolsoum, et al.
  Publicat: (2013)
• MEF2A sequence variants and coronary artery disease: a change of heart?
  per: Altshuler, David, et al.
  Publicat: (2005)