Biallelic variants in OGDH encoding oxoglutarate dehydrogenase lead to a neurodevelopmental disorder characterized by global developmental delay, movement disorder, and metabolic abnormalities
Ella F. Whittle(St George's, University of London), Christopher J. Carroll(St George's, University of London), Alan Pittman(St George's, University of London), Daniela Buhaş(McGill University Health Centre), Houda Zghal Elloumi, Shamima Rahman(Great Ormond Street Hospital for Children NHS Foundation Trust), Paria Najarzadeh Torbati, Helga Progri(Oklahoma Medical Research Foundation), Hui Yang, Erika Ignatius(University of Helsinki), Wan Hee Yoon(Oklahoma Medical Research Foundation), Sukyeong Lee(Baylor College of Medicine), Yalda Jamshidi(St George's, University of London), Melis Köse(Children's Hospital of Philadelphia), Madison Chilian(Oklahoma Medical Research Foundation), Ivan Shelihan(McGill University Health Centre), Ehsan Ghayoor Karimiani(St George's, University of London), Reza Shervin Badv(Children's Medical Center), Henry Houlden(Queen Mary University of London), Rebecca Ganetzky(Children's Hospital of Philadelphia), Reza Maroofian(University College London), Mehran Beiraghi Toosi(Mashhad University of Medical Sciences)
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