Magnetic resonance spectroscopy and molecular studies in ornithine transcarbamylase deficiency novel mutation c.802A>G in exon 8 (p.Met268Val)
Ewa Jamroz(Medical University of Silesia), Elżbieta Ciara(Children's Memorial Health Institute), Ewa Popowska(Instytut Matki i Dziecka), Justyna Paprocka(Medical University of Silesia), Maria Sokół(Centrum Onkologii)
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