University of Oxford-ko ikertzaileekin lankidetzan egindako argitalpenak (3)

2012

  1. Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry

    Nature Genetics

2010

  1. The first clinical case of a mutation at residue K185 of Kir6.2 (KCNJ11): A major ATP-binding residue

    Diabetic Medicine, Vol. 27, Núm. 2, pp. 225-229

2006

  1. Functional analysis of six Kir6.2 (KCNJ11) mutations causing neonatal diabetes

    Pflugers Archiv European Journal of Physiology, Vol. 453, Núm. 3, pp. 323-332