Concepedia

Congenital dyserythropoietic anemia type II: exclusion of seven candidate genes

Carmela Lanzara, Romina Ficarella, Xin Chen, Roberta Roberto, Silverio Perrotta, Carla Lasalandra, Paolo Gasparini, Achille Iolascon, Massimo Carella

Blood Cells Molecules and Diseases · 2003 · 21 citations · 18 references

DOI

Concepts

References

18

Oligosaccharyltransferase activity is associated with a protein complex composed of ribophorins I and II and a 48 kd protein

Daniel J. Kelleher, Gert Kreibich, Reid Gilmore · Cell · 1992 · 287 citations

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Hereditary Erythroblastic Multinuclearity Associated with a Positive Acidified‐Serum Test: a Type of Congenital Dyserythropoietic Anaemia

J. H. Crookston, Marie C. Crookston, Katherine L. Burnie et al. · British Journal of Haematology · 1969 · 215 citations

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Primary defect of congenital dyserythropoietic anemia type II. Failure in glycosylation of erythrocyte lactosaminoglycan proteins caused by lowered N-acetylglucosaminyltransferase II.

Michiko N. Fukuda, Anne Dell, Paolo Scartezzini · Journal of Biological Chemistry · 1987 · 105 citations · Full text

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Incomplete synthesis of N-glycans in congenital dyserythropoietic anemia type II caused by a defect in the gene encoding alpha-mannosidase II.

Michiko N. Fukuda, Khaled A. Masri, Anne Dell et al. · Proceedings of the National Academy of Sciences · 1990 · 103 citations

, , +16

Localization of the Congenital Dyserythropoietic Anemia II Locus to Chromosome 20q11.2 by Genomewide Search

Paolo Gasparini, Emanuele Miraglia del Giudice, J. Delaunay et al. · The American Journal of Human Genetics · 1997 · 100 citations · Full text

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