Ítems similars

• Spastin mutations are frequent in sporadic spastic paraparesis and their spectrum is different from that observed in familial cases
  per: Depienne, C, et al.
  Publicat: (2006)
• Missense mutations of ACTA1 cause dominant congenital myopathy with cores
  per: Kaindl, A, et al.
  Publicat: (2004)
• Novel mutations in the γ-crystallin genes cause autosomal dominant congenital cataracts
  per: Santhiya, S, et al.
  Publicat: (2002)
• Investigation of somatic NKX2-5 mutations in congenital heart disease
  per: Draus, J M, et al.
  Publicat: (2009)
• Linkage stratification and mutation analysis at the parkin locus identifies mutation positive Parkinson's disease families
  per: Nichols, W, et al.
  Publicat: (2002)