TY  - JOUR
AU  - Lamolda, Mar
AU  - Montes, Rosa
AU  - Simón, Iris
AU  - Perales, Sonia
AU  - Martínez-Navajas, Gonzalo
AU  - Lopez-Onieva, Lourdes
AU  - Ríos-Pelegrina, Rosa
AU  - Del Moral, Raimundo García
AU  - Griñan-Lison, Carmen
AU  - Marchal, Juan A
AU  - Lozano, Maria L
AU  - Ramos-Mejia, Veronica
AU  - Rivera, Jose
AU  - Bastida, Jose M
AU  - Real, Pedro J
PY  - 2019
DO  - 10.1016/j.scr.2019.101603
UR  - http://hdl.handle.net/10668/14652
T2  - Stem cell research
AB  - Familial Platelet Disorder with associated Myeloid Malignancy (FPDMM) is a rare platelet disorder caused by mutations in RUNX1. We generated an iPSC line (GENYOi005-A) from a FPDMM patient with a non-previously reported variant p.Thr196Ala....
LA  - en
KW  - Blood Coagulation Disorders, Inherited
KW  - Blood Platelet Disorders
KW  - Cell Differentiation
KW  - Cells, Cultured
KW  - Cellular Reprogramming
KW  - Core Binding Factor Alpha 2 Subunit
KW  - Female
KW  - Humans
KW  - Induced Pluripotent Stem Cells
KW  - Leukemia, Myeloid, Acute
KW  - Leukocytes, Mononuclear
KW  - Middle Aged
KW  - Mutation
TI  - GENYOi005-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with Familial Platelet Disorder with associated Myeloid Malignancy (FPDMM) carrying a p.Thr196Ala variant.
TY  - research article
VL  - 41
ER  -