• 2021 [x]

• Artikel [x]

• Protein Isoforms/genetics [MeSH] [x]
• Phenotype [MeSH] [x]
• Neurodevelopmental Disorders/genetics [MeSH] [x]
• Mutation, Missense/genetics [MeSH] [x]
• Male [MeSH] [x]
• Loss of Heterozygosity [MeSH] [x]
• Intellectual Disability/genetics [MeSH] [x]

Sacherschließung

• Original Article (1)
• Isoform-based phenotypic continuum (1)
• Intellectual disability (1)

Publikationstyp

Erscheinungsjahr

Institution