The Human Aminophospholipid-Transporting ATPase Gene ATP10C Maps Adjacent to UBE3A and Exhibits Similar Imprinted Expression
- 1 June 2001
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 68 (6) , 1501-1505
- https://doi.org/10.1086/320616
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Copper transport and its alterations in Menkes and Wilson diseasesPublished by Elsevier ,2001
- A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndromeNature Genetics, 2001
- Autism Spectrum DisordersPublished by Elsevier ,2000
- Genetic studies in autistic disorder and chromosome 15neurogenetics, 2000
- Mutation screening of the UBE3A /E6-AP gene in autistic disorderMolecular Psychiatry, 1999
- Linkage-Disequilibrium Mapping of Autistic Disorder, with 15q11-13 MarkersAmerican Journal of Human Genetics, 1998
- Inherited Interstitial Duplications of Proximal 15q: Genotype-Phenotype CorrelationsAmerican Journal of Human Genetics, 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
- Autism in Angelman syndrome: a population-based studyPediatric Neurology, 1996