mtDNA in congenital myotonic dystrophy.

Ítems similars

• Congenital myotonic dystrophy and mtDNA.
  per: Poulton, J
  Publicat: (1992)
• A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome.
  per: Noer, A S, et al.
  Publicat: (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
  per: Marzuki, Sangkot, et al.
  Publicat: (1992)
• MtDNA haplogroups in Native Americans.
  per: Torroni, A, et al.
  Publicat: (1995)
• mtDNA and the peopling of the Americas.
  per: Szathmary, E J
  Publicat: (1993)