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Publications by Birgitta Sander
Congenital Dyserythropoietic Anemia Type 1: A Case With Novel Compound Heterozygous Mutations in the C15orf41 Gene
American Journal of Hematology
Hematology
Perturbations of the Endocannabinoid System in Mantle Cell Lymphoma: Correlations to Clinical and Pathological Features
Oncoscience
Cancer Research
Oncology
Related publications
Codanin-1 Mutations in Congenital Dyserythropoietic Anemia Type 1 Affect HP1 Localization in Erythroblasts
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Congenital Dyserythropoietic Anemia Type III
Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene
Turkish Journal of Haematology
Hematology
Characterization of the Interactions Between Codanin-1 and C15Orf41, Two Proteins Implicated in Congenital Dyserythropoietic Anemia Type I Disease
BMC Molecular and Cell Biology
Cell Biology
Molecular Biology
Thrombocytopenia With Congenital Dyserythropoietic Anemia
Novel Compound Heterozygous COG5 Mutations in a Chinese Male Patient With Severe Clinical Symptoms and Type�IIi Congenital Disorder of Glycosylation: A Case Report
Experimental and Therapeutic Medicine
Medicine
Cancer Research
Immunology
Microbiology
A Novel Compound Heterozygous Mutation of the AIRE Gene in a Patient With Autoimmune Polyendocrine Syndrome Type 1
Annals of Pediatric Endocrinology and Metabolism
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
A Case of Congenital Dyserythropoietic Anemia Type 1 in a Japanese Adult With a CDAN1 Gene Mutation and an Inappropriately Low Serum Hepcidin-25 Level
Internal Medicine
Internal Medicine
Medicine
Compound Heterozygous Novel Frameshift Variants in the PROM1 Gene Result in Leber Congenital Amaurosis
Cold Spring Harbor molecular case studies
Biochemistry
Molecular Medicine
Genetics
