Mutational profiling of a MonoMAC syndrome family with GATA2 deficiency

Leukemia

Volumn 31, Issue 1, 2017, Pages 244-245

  Ding, L W ^a   Ikezoe, T ^b   Tan, K T ^a   Mori, M ^c   Mayakonda, A ^a   Chien, W ^a   Lin, D C ^a,d   Jiang, Y Y ^a   Lill, M ^d   Yang, H ^a   Sun, Q Y ^a   Koeffler, H P ^a,d  

^a NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

^b FUKUSHIMA MEDICAL UNIVERSITY   (Japan)

^c KOCHI UNIVERSITY   (Japan)

^d UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; TRANSCRIPTION FACTOR GATA 2;

AUTOSOMAL DOMINANT DISORDER; BONE MARROW; FEMALE; FRAMESHIFT MUTATION; HUMAN; HUMAN GENOME; HUMAN TISSUE; LETTER; MALE; MONOMAC SYNDROME; MYELODYSPLASTIC SYNDROME; NONSENSE MUTATION; PRIORITY JOURNAL; SOMATIC MUTATION; ADOLESCENT; DEFICIENCY; DNA MUTATIONAL ANALYSIS; GENETICS; GERMLINE MUTATION; MONOCYTE; MYELODYSPLASTIC SYNDROMES; PATHOLOGY; PEDIGREE;

ADOLESCENT; DNA MUTATIONAL ANALYSIS; FEMALE; GATA2 TRANSCRIPTION FACTOR; GERM-LINE MUTATION; HUMANS; MALE; MONOCYTES; MYELODYSPLASTIC SYNDROMES; PEDIGREE;

EID: 84992093450     PISSN: 08876924     EISSN: 14765551     Source Type: Journal    
DOI: 10.1038/leu.2016.256     Document Type: Letter

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