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ADAT3 Related Autosomal Recessive Intellectual Disability: A Case Report

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ajmg.a.37578openalex-extracted

ADAT3‐related intellectual disability: Further delineation of the phenotype

inferredcites →https://doi.org/10.1016/j.ejmg.2018.10.001openalex-extracted

A new case confirming and expanding the phenotype spectrum of ADAT3-related intellectual disability syndrome

inferredcites →https://doi.org/10.1016/s0300-9084(02)01446-3openalex-extracted

RNA editing by adenosine deaminases generates RNA and protein diversity

inferredcites →https://doi.org/10.1055/s-0039-1693151openalex-extracted

Novel Missense Variants in ADAT3 as a Cause of Syndromic Intellectual Disability

inferredcites →https://doi.org/10.1080/15476286.2017.1358348openalex-extracted

Codon adaptation to tRNAs with Inosine modification at position 34 is widespread among Eukaryotes and present in two Bacterial phyla

inferredcites →https://doi.org/10.1126/science.286.5442.1146openalex-extracted

An Adenosine Deaminase that Generates Inosine at the Wobble Position of tRNAs

inferredcites →https://doi.org/10.1128/mcb.00203-19openalex-extracted

Formation of tRNA Wobble Inosine in Humans Is Disrupted by a Millennia-Old Mutation Causing Intellectual Disability

inferredcites →https://doi.org/10.1136/jmedgenet-2012-101378openalex-extracted

Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus

inferredcites →https://doi.org/10.3390/ijms160817303openalex-extracted

Distribution of ADAT-Dependent Codons in the Human Transcriptome

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