High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia

Blood

Volumn 121, Issue 5, 2013, Pages 822-829

  Pasquet, Marlène ^a   Bellanné Chantelot, Christine ^b   Tavitian, Suzanne ^a,c   Prade, Naïs ^a   Beaupain, Blandine ^d   LaRochelle, Olivier ^a,e   Petit, Arnaud ^e   Rohrlich, Pierre ^f   Ferrand, Christophe ^f   Van Den Neste, Eric ^g   Poirel, Hélène A ^g   Lamy, Thierry ^h   Ouachée Chardin, Marie ⁱ   Mas, Véronique Mansat De ^a,c,j   Corre, Jill ^a,c,j   Récher, Christian ^a,c,j   Plat, Geneviève ^a   Bachelerie, Françoise ^k   Donadieu, Jean ^d,e   Delabesse, Eric ^a,c,j  

^a CHU PURPAN   (France)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^c CANCER RESEARCH CENTER OF TOULOUSE   (France)

^d ARMAND TROUSSEAU HOSPITAL   (France)

^e LAVAL UNIVERSITY   (Canada)

^f UNIVERSITÉ DE FRANCHE COMTÉ   (France)

^g CLINIQUES UNIVERSITAIRES SAINT LUC   (Belgium)

^h PONTCHAILLOU UNIVERSITY HOSPITAL   (France)

ⁱ HÔPITAL ROBERT DEBRÉ   (France)

^j UNIVERSITÉ DE TOULOUSE   (France)

^k INSERM   (France)

more..

Author keywords

Mutations of key transcription factor in myeloid malignancies

Indexed keywords

ALANINE; ANTINEOPLASTIC AGENT; ARGININE; GLUTAMIC ACID; GLUTAMINE; METHIONINE; THREONINE; TRANSCRIPTION FACTOR GATA 2; VALINE;

ACUTE GRANULOCYTIC LEUKEMIA; ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CANCER CHEMOTHERAPY; CANCER PATIENT; CHILD; CHRONIC NEUTROPENIA; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; DISEASE ASSOCIATION; EXOME; EXOME SEQUENCING; FAMILY HISTORY; FEMALE; GENE DELETION; GENE FREQUENCY; GENE LOCUS; GENE MUTATION; HEMATOLOGIC DISEASE; HUMAN; MALE; MONOCYTOPENIA; MONOMAC SYNDROME; MYELODYSPLASTIC SYNDROME; NEUTROPENIA; PATHOPHYSIOLOGY; PEDIGREE; PRIORITY JOURNAL; SCHOOL CHILD; SCREENING TEST; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84873530537     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2012-08-447367     Document Type: Article

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