Erratum: X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutations [Am. J. Hematol. 89 (2014) 315-319] DOI: 10.1002/ajh.23616;X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutations

American Journal of Hematology

Volumn 89, Issue 3, 2014, Pages 315-319

  Campagna, Dean R ^a   de Bie, Charlotte I ^b   Schmitz Abe, Klaus ^a   Sweeney, Marion ^c   Sendamarai, Anoop K ^a   Schmidt, Paul J ^a   Heeney, Matthew M ^a   Yntema, Helger G ^d   Kannengiesser, Caroline ^e   Grandchamp, Bernard ^e   Niemeyer, Charlotte M ^f   Knoers, Nine V A M ^b   Swart, Sonia ^g   Marron, Gordon ^h   van Wijk, Richard ^b   Raymakers, Reinier A ^b   May, Alison ^c   Markianos, Kyriacos ^a   Bottomley, Sylvia S ⁱ   Swinkels, Dorine W ^d   Fleming, Mark D ^a   more..

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^c CARDIFF UNIVERSITY SCHOOL OF MEDICINE   (United Kingdom)

^d RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^e BICHAT HOSPITAL   (France)

^f UNIVERSITY OF FREIBURG   (Germany)

^g NORTHAMPTON GENERAL HOSPITAL   (United Kingdom)

^h NINEWELLS HOSPITAL   (United Kingdom)

ⁱ UNIVERSITY OF OKLAHOMA COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

5 AMINOLEVULINATE SYNTHASE; 5 AMINOLEVULINATE SYNTHASE 2; PYRIDOXINE; TRANSCRIPTION FACTOR GATA; TRANSCRIPTION FACTOR GATA 1; TRANSCRIPTION FACTOR GATA 2; TRANSCRIPTION FACTOR GATA 3; TRANSCRIPTION FACTOR TAL1; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; ARTICLE; BINDING SITE; CLINICAL ARTICLE; DIET SUPPLEMENTATION; ENHANCER REGION; FEMALE; GATA BINDING SITE; GENE EXPRESSION; GENE MUTATION; GENETIC SCREENING; HUMAN; INTRON; MALE; MISSENSE MUTATION; PRIORITY JOURNAL; SITE DIRECTED MUTAGENESIS; UPREGULATION; X CHROMOSOME LINKAGE; X LINKED SIDEROBLASTIC ANEMIA;

5-AMINOLEVULINATE SYNTHETASE; ADULT; AGED; ANEMIA, SIDEROBLASTIC; BINDING SITES; ENHANCER ELEMENTS, GENETIC; EUROPE; FEMALE; GATA TRANSCRIPTION FACTORS; GENETIC DISEASES, X-LINKED; GENOTYPE; HUMANS; INTRONS; MALE; MIDDLE AGED; MUTATION; PEDIGREE; YOUNG ADULT;

EID: 84896828347     PISSN: 03618609     EISSN: 10968652     Source Type: Journal    
DOI: 10.1002/ajh.23741     Document Type: Erratum

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