Functional analysis of myosin missense mutations in familial hypertrophic cardiomyopathy.

Những quyển sách tương tự

• Functional analysis of myosin mutations that cause familial hypertrophic cardiomyopathy.
  Bằng: Roopnarine, O, et al.
  Được phát hành: (1998)
• Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.
  Bằng: Solomon, S D, et al.
  Được phát hành: (1990)
• Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.
  Bằng: Watkins, H, et al.
  Được phát hành: (1992)
• Medical genetics: advances in brief: Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy
  Bằng: Norman, Andrew
  Được phát hành: (1992)
• Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function
  Bằng: Schmitt, Joachim P., et al.
  Được phát hành: (2006)