Magnetic resonance spectroscopy and molecular studies in ornithine transcarbamylase deficiency novel mutation c.802A>G in exon 8 (p.Met268Val)Ewa Jamroz, Elżbieta Ciara, Justyna Paprocka et al.|Neurologia i Neurochirurgia Polska|2013Cited by 2
Xp21.2 contiguous gene syndrome due to deletion involving glycerol kinase and Duchenne muscular dystrophy lociJustyna Paprocka, Maciej Adamowicz, Ewa Jamroz et al.|Neurology India|2010Cited by 2
Xp21.2 contiguous gene syndrome due to deletion involving glycerolkinase and Duchenne muscular dystrophy lociEwa Jamroz, Maciej Adamowicz, Justyna Paprocka et al.|TSpace (University of Toronto)|2010Cited by 0