Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons
- 1 September 1997
- journal article
- letter
- Published by Springer Science and Business Media LLC in Nature Genetics
- Vol. 17 (1), 75-78
- https://doi.org/10.1038/ng0997-75
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- The E6–AP Ubiquitin–Protein Ligase (UBE3A) Gene Is Localized within a Narrowed Angelman Syndrome Critical RegionGenome Research, 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
- Angelman syndromeCurrent Problems in Pediatrics, 1995
- Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15Nature Genetics, 1995
- Imprinting analysis of three genes in the Prader — Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E)Human Molecular Genetics, 1994
- Cytogenetic and molecular analysis in Angelman syndromeAmerican Journal of Medical Genetics, 1993
- Maternal origin of 15q11–13 deletions in Angelman syndrome suggests a role for genomic imprintingAmerican Journal of Medical Genetics, 1990
- Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletionAmerican Journal of Medical Genetics, 1989
- Is angelman syndrome an alternate result of del(15)(qllql3)?American Journal of Medical Genetics, 1987