GATA1 mutation and trisomy 21 are required only in haematopoietic cells for development of transient myeloproliterative disorder

British Journal of Haematology

Volumn 128, Issue 4, 2005, Pages 548-551

  Carpenter, Emily ^a,b   Valverde Garduno, Veronica ^a   Sternberg, Alex ^a   Mitchell, Chris ^b   Roberts, Irene ^c   Vyas, Paresh ^a   Vora, Ajay ^d  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b OXFORD UNIVERSITY HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

^c HAMMERSMITH HOSPITAL   (United Kingdom)

^d SHEFFIELD CHILDREN S HOSPITAL   (United Kingdom)

Author keywords

Acute megakaryocytic leukaemia; GATA1; Transient myeloproliferative disorder; Trisomy 21

Indexed keywords

DNA; TRANSCRIPTION FACTOR GATA 1;

ACUTE MEGAKARYOCYTIC LEUKEMIA; ARTICLE; BLOOD CELL; CASE REPORT; CELL TYPE; CHILD; DOWN SYNDROME; FEMALE; GENE MUTATION; GENETIC PREDISPOSITION; HEMATOPOIETIC CELL; HUMAN; MALE; MYELOPROLIFERATIVE DISORDER; NEWBORN; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PRIORITY JOURNAL;

BASE SEQUENCE; CHROMOSOMES, HUMAN, PAIR 21; DNA MUTATIONAL ANALYSIS; DNA, NEOPLASM; DNA-BINDING PROTEINS; ERYTHROID-SPECIFIC DNA-BINDING FACTORS; FEMALE; GATA1 TRANSCRIPTION FACTOR; HUMANS; INFANT, NEWBORN; LEUKEMIA, MEGAKARYOCYTIC, ACUTE; MALE; MOLECULAR SEQUENCE DATA; MUTATION; MYELOPROLIFERATIVE DISORDERS; NEOPLASM PROTEINS; TRANSCRIPTION FACTORS; TRISOMY;

EID: 14144251673     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2004.05342.x     Document Type: Article

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