Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation.

Benzer Materyaller

• A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies.
  Yazar:: Moreira, E S, ve diğerleri
  Baskı/Yayın Bilgisi: (1998)
• Estimate of germinal mosaicism in Duchenne muscular dystrophy.
  Yazar:: Passos-Bueno, M R, ve diğerleri
  Baskı/Yayın Bilgisi: (1990)
• A model to estimate the expression of the dystrophin gene in muscle from female Becker muscular dystrophy carriers.
  Yazar:: Vainzof, M, ve diğerleri
  Baskı/Yayın Bilgisi: (1992)
• High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy families.
  Yazar:: Zatz, M, ve diğerleri
  Baskı/Yayın Bilgisi: (1995)
• The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12.
  Yazar:: Moreira, E S, ve diğerleri
  Baskı/Yayın Bilgisi: (1997)