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Biallelic variants in OGDH encoding oxoglutarate dehydrogenase lead to a neurodevelopmental disorder characterized by global developmental delay, movement disorder, and metabolic abnormalities
Document Type
Article
Author
Whittle, E.F.; Karimiani, E.G.; Jamshidi, Y.; Pittman, A.M.; Maroofian, R.; Carroll, C.J.; Chilian, M.; Progri, H.; Yoon, W.H.; Buhas, D.; Kose, M.; Ganetzky, R.D.; Toosi, M.B.; Torbati, P.N.; Badv, R.S.; Shelihan, I.; Yang, H.; Elloumi, H.Z.; Lee, S.; Houlden, H.; Ignatius, E.; Rahman, S.
Source
In: Genetics in Medicine. (Genetics in Medicine, February 2023, 25(2))
Subject
Language
English
ISSN
15300366
10983600

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