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Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome.
Am J Hum Genet. 2024 Jan 4;111(1):200-210. doi: 10.1016/j.ajhg.2023.11.012. Epub 2023 Dec 20.
Am J Hum Genet. 2024.
PMID: 38118446
Free PMC article.
Maintenance of neuronal fate and transcriptional identity.
Aughey GN.
Aughey GN.
Biol Open. 2023 Jun 15;12(6):bio059953. doi: 10.1242/bio.059953. Epub 2023 Jun 5.
Biol Open. 2023.
PMID: 37272626
Free PMC article.
Review.
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