Rare combination of dilated cardiomyopathy and ankylosing spondylitis in a family

Ítems similars

• Heterozygous desmin gene (DES) mutation contributes to familial dilated cardiomyopathy
  per: Huang, Ying-shuo, et al.
  Publicat: (2021)
• Familial dilated cardiomyopathy—not so rare
  per: McKenna, William J
  Publicat: (1992)
• A Rare Co-Segregation-Mutation in the Insulin Receptor Substrate 1 Gene in One Chinese Family with Ankylosing Spondylitis
  per: Rong, Ju, et al.
  Publicat: (2015)
• Transfer Dysphagia in a Patient With the Rare Combination of Scleroderma and Ankylosing Spondylitis
  per: Witt, Peter, et al.
  Publicat: (1987)
• The Familial Occurrence of Ankylosing Spondylitis
  per: Jacobs, J. H., et al.
  Publicat: (1954)