Severe neurological manifestations in an Egyptian patient with a novel frameshift mutation in the Glutaryl-CoA dehydrogenase gene
Crossref DOI link: https://doi.org/10.1007/s11011-016-9879-x
Published Online: 2016-08-01
Published Print: 2017-02
Update policy: https://doi.org/10.1007/springer_crossmark_policy
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
Funding for this research was provided by:
Qatar University (QUUG-CAS-DHS-14/15-3)
License valid from 2016-08-01