A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11-q12

類似資料

• Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.
  著者:: Solomon, S D, 等
  出版事項: (1990)
• Functional analysis of myosin missense mutations in familial hypertrophic cardiomyopathy.
  著者:: Straceski, A J, 等
  出版事項: (1994)
• Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy.
  著者:: Watkins, H, 等
  出版事項: (1993)
• Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.
  著者:: Watkins, H, 等
  出版事項: (1992)
• Syncope in hypertrophic cardiomyopathy.
  著者:: McKenna, W, 等
  出版事項: (1982)