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Institut für Humangenetik der Universitätsmedizin Göttingen Institut für Humangenetik der Universitätsmedizin Göttingen
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Archives

Monthly Archive for: "July, 2022"
Home » Archiv für July 2022
By KB
In News, Research
Posted 29. July 2022

Biallelic WARS1 variants identified as genetic cause of neurodevelopmental syndrome

WARS1 is one of many key enzymes required for protein synthesis. Genetic variants in WARS1 are rare, with extremely limited evidence implicating it in a clinically heterogeneous autosomal [...]

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By KB
In News, Research
Posted 20. July 2022

Identified biallelic variants in tRNA synthetases reveal an emerging associated disease spectrum

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By KB
In Gene of the Month
Posted 4. July 2022

Gene of the Month – June: SLC47A1

Loss-of-function variants in SLC47A1 play a causal role in the development of kidney disease. This is one of the results generated by an extensive metaanalysis of genome-wide association studies [...]

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