Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy.

Samankaltaisia teoksia

• Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy.
  Tekijä: Watkins, H, et al.
  Julkaistu: (1993)
• Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.
  Tekijä: Watkins, H, et al.
  Julkaistu: (1992)
• Detection of a new mutation in the beta-myosin heavy chain gene in an individual with hypertrophic cardiomyopathy.
  Tekijä: Marian, A J, et al.
  Julkaistu: (1992)
• A Novel Mutation of the Beta Myosin Heavy Chain Gene Responsible for Familial Hypertrophic Cardiomyopathy
  Tekijä: Wang, Juan, et al.
  Julkaistu: (2009)
• Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy.
  Tekijä: Fananapazir, L, et al.
  Julkaistu: (1993)