N-terminal 152 amino-acid residue-long domain of DHX30 (DHX30N), which... | Download Scientific Diagram
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Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders | Genome Medicine | Full Text
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A Japanese adult and two girls with NEDMIAL caused by de novo missense variants in DHX30 | Human Genome Variation
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The RNA helicase DHX30 coordinates cytoplasmic translation and mitochondrial function contributing to cancer cell survival | bioRxiv
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Nutlin-Induced Apoptosis Is Specified by a Translation Program Regulated by PCBP2 and DHX30 - ScienceDirect
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Cureus | A Novel De Novo Mutation of the DHX30 Gene in a Patient With Neurodevelopmental Disorder, Severe Motor Impairment, and Absent Language (NEDMIAL) | Article
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Devastating Diagnosis: Children with rare mutation meet for first time in Fort Lauderdale – WSVN 7News | Miami News, Weather, Sports | Fort Lauderdale
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Cancers | Free Full-Text | DHX30 Coordinates Cytoplasmic Translation and Mitochondrial Function Contributing to Cancer Cell Survival
De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder
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Conformational change of RNA-helicase DHX30 by ALS/FTD-linked FUS induces mitochondrial dysfunction and cytosolic aggregates | Scientific Reports
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Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders | Genome Medicine | Full Text
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Conformational change of RNA-helicase DHX30 by ALS/FTD-linked FUS induces mitochondrial dysfunction and cytosolic aggregates | Scientific Reports
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