Eitemau Tebyg

• A tRNA(Ala) mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy
  gan: Horvath, R, et al.
  Cyhoeddwyd: (2003)
• Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene
  gan: Horvath, R, et al.
  Cyhoeddwyd: (2002)
• Novel mutations in the γ-crystallin genes cause autosomal dominant congenital cataracts
  gan: Santhiya, S, et al.
  Cyhoeddwyd: (2002)
• Genetic, functional, and histopathological evaluation of two C‐terminal BRCA1 missense variants
  gan: Lovelock, P K, et al.
  Cyhoeddwyd: (2006)
• Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome
  gan: Plasilova, M, et al.
  Cyhoeddwyd: (2004)