Severe neurological manifestations in an Egyptian patient with a novel frameshift mutation in the Glutaryl-CoA dehydrogenase gene
Moseilhy, Ahmed, Hassan, Magdy M., El Abd, Heba S. A., Mohammad, Shaimaa A., El Bekay, Rajaa, Abdel-Motal, Ussama M., Ouhtit, Allal, Zaki, Osama K., Zayed, Hatem
Published in Metabolic brain disease (01.02.2017)
Published in Metabolic brain disease (01.02.2017)
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