mtDNA in congenital myotonic dystrophy.

Podobne zapisy

• Congenital myotonic dystrophy and mtDNA.
  od: Poulton, J
  Wydane: (1992)
• A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome.
  od: Noer, A S, i wsp.
  Wydane: (1991)
• Reply to Howell et al.: The need for a joint effort in the construction of a reference data base for normal sequence variants of human mtDNA
  od: Marzuki, Sangkot, i wsp.
  Wydane: (1992)
• mtDNA and the peopling of the Americas.
  od: Szathmary, E J
  Wydane: (1993)
• MtDNA haplogroups in Native Americans.
  od: Torroni, A, i wsp.
  Wydane: (1995)