Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function

<p dir="ltr">Aminoacyl-tRNA synthetases (ARSs) are essential enzymes for faithful assignment of amino acids to their cognate tRNA. Variants in ARS genes are frequently associated with clinically heterogeneous phenotypes in humans and follow both autosomal dominant or recessive inheri...

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Main Author:	Sheng‐Jia Lin (18877600) (author)
Other Authors:	Barbara Vona (5237843) (author), Hillary M. Porter (18877603) (author), Mahmoud Izadi (12899508) (author), Kevin Huang (147764) (author), Yves Lacassie (6034238) (author), Jill A. Rosenfeld (9606199) (author), Saadullah Khan (5735540) (author), Cassidy Petree (17487198) (author), Tayyiba A. Ali (18131836) (author), Nazif Muhammad (15891860) (author), Sher A. Khan (18877606) (author), Noor Muhammad (820180) (author), Pengfei Liu (136115) (author), Marie‐Louise Haymon (18877609) (author), Franz Rüschendorf (73756) (author), Il‐Keun Kong (18877612) (author), Linda Schnapp (18718837) (author), Natasha Shur (18877615) (author), Lynn Chorich (18877618) (author), Lawrence Layman (3521192) (author), Thomas Haaf (342924) (author), Ehsan Pourkarimi (541179) (author), Hyung‐Goo Kim (14776987) (author), Gaurav K. Varshney (10671462) (author)
Published:	2022
Subjects:	Biomedical and clinical sciences Clinical sciences Neurosciences autosomal recessive biallelic variants C. elegans translation initiation sites tryptophanyl‐tRNA synthetase 1 (WARS1) WHEP domain zebrafish
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Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function

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