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A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome.
Barrientos Rubio, Antoni; Volpini Bertrán, Victor; Casademont i Pou, Jordi; Genís, David; Manzanares, Josep-Maria; Ferrer, Isidro (Ferrer Abizanda); Corral, J.; Cardellach, Francesc; Urbano Márquez, A. (Álvaro); Estivill, Xavier, 1955-; Nunes Martínez, Virginia
Universitat de Barcelona
2010-05-04
Mitocondris
Degeneració del sistema nerviòs
Genètica humana
Neurodegenerative disease
OXPHOS
Autosomal recessive inheritance
Linkage
DIDMOAD
(c) The American Society for Clinical Investigation, 1996
Article
American Society for Clinical Investigation
         

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