Localization of the Congenital Dyserythropoietic Anemia II Locus to Chromosome 20q11.2 by Genomewide Search
- 1 November 1997
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 61 (5) , 1112-1116
- https://doi.org/10.1086/301609
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- A comprehensive genetic map of the human genome based on 5,264 microsatellitesNature, 1996
- Molecular cloning and expression of cDNAs encoding human alpha-mannosidase II and a previously unrecognized alpha-mannosidase IIx isozyme.Proceedings of the National Academy of Sciences, 1995
- The human UDP-N-Acetylglucosamine:alpha-6-d-Mannoside-beta-1,2-N-Acetylglucosaminyltransferase II Gene (MGAT2). Cloning of Genomic DNA, Localization to Chromosome 14q21, Expression in Insect Cells and Purification of the Recombinant ProteinEuropean Journal of Biochemistry, 1995
- Localization of the gene for congenital dyserythropoietic anemia type III, CDAN3, to chromosome 15q21-q25Human Molecular Genetics, 1995
- The 1993–94 Généthon human genetic linkage mapNature Genetics, 1994
- Isolation, characterization, and expression of cDNAs encoding murine alpha-mannosidase II, a Golgi enzyme that controls conversion of high mannose to complex N-glycans.The Journal of cell biology, 1991
- Incomplete synthesis of N-glycans in congenital dyserythropoietic anemia type II caused by a defect in the gene encoding alpha-mannosidase II.Proceedings of the National Academy of Sciences, 1990
- HEMPAS disease: genetic defect of glycosylationGlycobiology, 1990
- Congenital Dyserythropoietic Anaemia, Types I and II: Aberrant Pattern of Erythrocyte Membrane Proteins in CDA II, as Revealed by Two‐dimensional Polyacrylamide Gel ElectrophoresisBritish Journal of Haematology, 1977
- Hereditary Erythroblastic Multinuclearity Associated with a Positive Acidified‐Serum Test: a Type of Congenital Dyserythropoietic AnaemiaBritish Journal of Haematology, 1969