Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population

  1. González-Vioque, E.
  2. Blázquez, A.
  3. Fernández-Moreira, D.
  4. Bornstein, B.
  5. Bautista, J.
  6. Arpa, J.
  7. Navarro, C.
  8. Campos, Y.
  9. Fernández-Moreno, M.A.
  10. Garesse, R.
  11. Arenas, J.
  12. Martín, M.A.
Aldizkaria:
Archives of Neurology

ISSN: 0003-9942 1538-3687

Argitalpen urtea: 2006

Alea: 63

Zenbakia: 1

Orrialdeak: 107-111

Mota: Artikulua

DOI: 10.1001/ARCHNEUR.63.1.107 GOOGLE SCHOLAR lock_openSarbide irekia editor

Garapen Iraunkorreko Helburuak