Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons

This publication has 19 references indexed in Scilit:

• The E6–AP Ubiquitin–Protein Ligase (UBE3A) Gene Is Localized within a Narrowed Angelman Syndrome Critical Region
  Genome Research, 1997
• De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome
  Nature Genetics, 1997
• UBE3A/E6-AP mutations cause Angelman syndrome
  Nature Genetics, 1997
• Angelman syndrome
  Current Problems in Pediatrics, 1995
• Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15
  Nature 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 syndrome
  American Journal of Medical Genetics, 1993
• Maternal origin of 15q11–13 deletions in Angelman syndrome suggests a role for genomic imprinting
  American Journal of Medical Genetics, 1990
• Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion
  American Journal of Medical Genetics, 1989
• Is angelman syndrome an alternate result of del(15)(qllql3)?
  American Journal of Medical Genetics, 1987