Biallelic variants in OGDH encoding oxoglutarate dehydrogenase lead to a neurodevelopmental disorder characterized by global developmental delay, movement disorder, and metabolic abnormalities-Reference-Cited by-同舟云学术

Biallelic variants in OGDH encoding oxoglutarate dehydrogenase lead to a neurodevelopmental disorder characterized by global developmental delay, movement disorder, and metabolic abnormalities

Published:2023-02 Issue:2 Volume:25 Page:100332
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Whittle Ella F.^ORCID,Chilian Madison,Karimiani Ehsan Ghayoor,Progri Helga,Buhas Daniela,Kose Melis,Ganetzky Rebecca D.,Toosi Mehran Beiraghi,Torbati Paria Najarzadeh,Badv Reza Shervin,Shelihan Ivan,Yang Hui,Elloumi Houda Zghal,Lee Sukyeong,Jamshidi Yalda,Pittman Alan M.,Houlden Henry,Ignatius Erika,Rahman Shamima,Maroofian Reza,Yoon Wan Hee^ORCID,Carroll Christopher J.^ORCID

Publisher

Elsevier BV

Subject

Genetics (clinical)

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