Biochemical Analysis of Angelman Syndrome-associated Mutations in the E3 Ubiquitin Ligase E6-associated Protein
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference30 articles.
1. Angelman syndrome: a review of clinical and genetic aspects
2. UBE3A/E6-AP mutations cause Angelman syndrome
3. De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome
4. Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons
5. The Angelman syndrome candidate gene, UBE3AIE6-AP, is imprinted in brain
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