检索结果 - Anuradha Ganesh
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THUMPD1 bi-allelic variants cause loss of tRNA acetylation and a syndromic neurodevelopmental disorder 由 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 Bézieau, Dragony Fu, Bertrand Isidor, Benjamin Cogné, Mitchell R. O’Connell
出版 2022Artigo
相关主题
Acetylation
Allele
Biology
Cohort
Esotropia
Exotropia
Gene
Genetics
Incidence (geometry)
Intellectual disability
Internal medicine
Loss function
Medicine
Messenger RNA
Missense mutation
Optics
Orthoptic
Phenotype
Physics
RNA
Retrospective cohort study
Strabismus
Strabismus surgery
Surgery
Transfer RNA
Translation (biology)
Visual acuity