Rearrangement of VPS13B, a causative gene of Cohen syndrome, in a case of RUNX1-RUNX1T1 leukemia with t(8;12;21).
Int J Hematol
; 108(2): 208-212, 2018 Aug.
Article
in En
| MEDLINE
| ID: mdl-29264741
Full text:
1
Database:
MEDLINE
Main subject:
Translocation, Genetic
/
Chromosomes, Human, Pair 8
/
Chromosomes, Human, Pair 12
/
Chromosomes, Human, Pair 21
/
Gene Rearrangement
/
Leukemia, Myeloid, Acute
/
Vesicular Transport Proteins
/
Core Binding Factor Alpha 2 Subunit
/
Fingers
/
RUNX1 Translocation Partner 1 Protein
Limits:
Female
/
Humans
/
Middle aged
Language:
En
Journal:
Int J Hematol
Journal subject:
HEMATOLOGIA
Year:
2018
Type:
Article
Affiliation country:
Japan