Ribosome defects in disorders of erythropoiesis

International Journal of Hematology

Volumn 93, Issue 2, 2011, Pages 144-149

  Narla, Anupama ^a,b,c   Hurst, Slater N ^b   Ebert, Benjamin L ^a,b,d  

^a HARVARD MEDICAL SCHOOL   (United States)

^b BRIGHAM AND WOMEN S HOSPITAL   (United States)

^c BOSTON CHILDREN S HOSPITAL   (United States)

^d HARVARD STEM CELL INSTITUTE   (United States)

Author keywords

Diamond Blackfan anemia; Myelodysplastic syndrome; p53

Indexed keywords

ADENOSINE DEAMINASE; PROTEIN MDM2; PROTEIN P53; RIBOSOME DNA; RIBOSOME PROTEIN; RIBOSOME PROTEIN S14; RIBOSOME PROTEIN S19; UNCLASSIFIED DRUG;

5Q- SYNDROME; ARTICLE; BLACKFAN DIAMOND ANEMIA; BONE MARROW DEPRESSION; DYSERYTHROPOIESIS; GENE; HETEROZYGOSITY LOSS; HUMAN; LOSS OF FUNCTION MUTATION; MACROCYTIC ANEMIA; MANDIBULOFACIAL DYSOSTOSIS; MISSENSE MUTATION; MYELODYSPLASTIC SYNDROME; NONHUMAN; RETICULOCYTOPENIA; RIBOSOMAL PROTEIN S19 GENE; RIBOSOME; RIBOSOME PROTEIN S14 GENE; TCOF1 GENE; THROMBOCYTOSIS;

ANEMIA, APLASTIC; ANEMIA, DIAMOND-BLACKFAN; HUMANS; METABOLIC DISEASES; RIBOSOMAL PROTEINS; RIBOSOMES;

EID: 79952250933     PISSN: 09255710     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12185-011-0776-0     Document Type: Article

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