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5 Einträge gefunden

Mutations in genes encoding regulators of mRNA decapping and translation initiation: links to intellectual disability
2020 - Forschungsinformationssystem des UKE
Germline AGO2 mutations impair RNA interference and human neurological development
2020 - Forschungsinformationssystem des UKE
Nine newly identified individuals refine the phenotype associated with MYT1L mutations
2020 - Forschungsinformationssystem des UKE
MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis
2020 - Forschungsinformationssystem des UKE
Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology
2020 - Forschungsinformationssystem des UKE