Sökresultat - Berti, Gianna

  • Visas 1 - 1 av 1 resultat
Förfina resultatet
  1. 1
    A novel mutation in the mitochondrial tRNA(Pro) gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiency

    A novel mutation in the mitochondrial tRNA(Pro) gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiency av Da Pozzo, Paola, Cardaioli, Elena, Malfatti, Edoardo, Gallus, Gian Nicola, Malandrini, Alessandro, Gaudiano, Carmen, Berti, Gianna, Invernizzi, Federica, Zeviani, Massimo, Federico, Antonio

    Publicerad 2009
    Hämta fulltext Hämta fulltext Hämta fulltext
    Text
    Lägg till i favoriter
    Sparad:

Sökverktyg: