The Angelman syndrome candidate gene, UBE3AIE6-AP, is imprinted in brain
- 1 September 1997
- journal article
- Published by Springer Nature in Nature Genetics
- Vol. 17 (1) , 14-15
- https://doi.org/10.1038/ng0997-14
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- The HumanE6-APGene (UBE3A) Encodes Three Potential Protein Isoforms Generated by Differential SplicingGenomics, 1997
- De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndromeNature Genetics, 1997
- UBE3A/E6-AP mutations cause Angelman syndromeNature Genetics, 1997
- Cloning and characterization of the human homologue of a dystrophin related phosphoprotein found at the Torpedo electric organ post- synaptic membraneHuman Molecular Genetics, 1996
- Imprinting analysis of three genes in the Prader — Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E)Human Molecular Genetics, 1994
- Puppet‐like syndrome of AngelmanNeurology, 1991