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Severe neurological manifestations in an Egyptian patient with a novel frameshift mutation in the Glutaryl-CoA dehydrogenase gene
Ahmed Moseilhy, Magdy M. Hassan, Heba S.A. El Abd, Shaimaa A. Mohammad, Rajaa El Bekay, Ussama M. Abdel-Motal, Allal Ouhtit, Osama K. Zaki*, Hatem Zayed
*Corresponding author for this work
Research output: Contribution to journal › Article › peer-review
7
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(Scopus)