Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1
- 1 December 2002
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 71 (6) , 1467-1474
- https://doi.org/10.1086/344781
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Mechanical Implications of the Domain Structure of Fiber-Forming Collagens: Comparison of the Molecular and Fibrillar Flexibilities of the α1-Chains Found in Types I–III CollagenJournal of Theoretical Biology, 2002
- Ripping up the nuclear envelopeNature, 2002
- A Recessive Contiguous Gene Deletion of Chromosome 2p16 Associated with Cystinuria and a Mitochondrial DiseaseAmerican Journal of Human Genetics, 2001
- Consistency analysis of similarity between multiple alignments: prediction of protein function and fold structure from analysis of local sequence motifsJournal of Molecular Biology, 2001
- Severe congenital dyserythropoietic anaemia type I: prenatal management, transfusion support and alpha‐interferon therapyBritish Journal of Haematology, 2000
- The congenital dyserythropoietic anaemiasBest Practice & Research Clinical Haematology, 1999
- Reduced interferon‐alpha production by Epstein‐Barr virus transformed B‐lymphoblastoid cell lines and lectin‐stimulated lymphocytes in congenital dyserythropoietic anaemia type IBritish Journal of Haematology, 1997
- Alpha-interferon therapy for congenital dyserythropoiesis type IBritish Journal of Haematology, 1995
- Basic local alignment search toolJournal of Molecular Biology, 1990
- The microtubule binding domain of microtubule-associated protein MAP1B contains a repeated sequence motif unrelated to that of MAP2 and tau.The Journal of cell biology, 1989