Documentos relacionados

1. [Autosomal dominant mental retardation type 5 caused by <i>SYNGAP1</i> gene mutations: a report of 8 cases and literature review].
2. [Correlation of early neurodevelopmental features of children with SYNGAP1 variants and their genotypes].
3. Novel Mutation of SYNGAP1 Associated with Autosomal Dominant Mental Retardation 5 in a Chinese Patient.
4. Molecular and phenotypical findings of a novel de novo SYNGAP1 gene variant in an 11-year-old Iranian boy with intellectual disability.
5. [A case of mental retardation caused by a frameshift variant of SYNGAP1 gene].
6. [Identification of a novel SYNGAP1 mutation in a child with intellectual disability].
7. DAB2IP down-regulates HSP90AA1 to inhibit the malignant biological behaviors of colorectal cancer.
8. [A case with autosomal dominant mental retardation type 5 due to de novo SYNGAP1 variant].
9. Species-conserved SYNGAP1 phenotypes associated with neurodevelopmental disorders.
10. CDC42-IQGAP Interactions Scrutinized: New Insights into the Binding Properties of the GAP-Related Domain.