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THUMPD1 bi-allelic variants cause loss of tRNA acetylation and a syndromic neurodevelopmental disorder

Martin Broly, Bogdan Polevoda, Kamel Awayda, Ning Tong, Jenna M. Lentini, Thomas Besnard, Wallid Deb, Declan O’Rourke, Júlia Baptista, Sian Ellard, Mohammed Almannai, Mais Hashem, Ferdous Abdulwahab, Hanan E. Shamseldin, Saeed M Al-Tala, Fowzan S. Alkuraya, A. S. Leon, Rosa Laura E. van Loon, Alessandra Ferlini, Mariabeatrice Sanchini, Stefania Bigoni, Andrea Ciorba, Hans van Bokhoven, Zafar Iqbal, Almundher Al‐Maawali, Fathiya Al-Murshedi, Anuradha Ganesh, Watfa Al‐Mamari, Sze Chern Lim, Lynn Pais, Natasha J. Brown, Saima Riazuddin, Stéphane Bezieau, Dragony Fu, Bertrand Isidor, Benjamin Cogné, Mitchell R. O’Connell

2022The American Journal of Human Genetics47 citationsDOIOpen Access PDF

Topics & Concepts

Transfer RNAGeneticsLoss functionBiologyMissense mutationAlleleGeneAcetylationIntellectual disabilityPhenotypeTranslation (biology)RNAMessenger RNARNA modifications and cancerPeptidase Inhibition and AnalysisRNA and protein synthesis mechanisms
THUMPD1 bi-allelic variants cause loss of tRNA acetylation and a syndromic neurodevelopmental disorder | Litcius