TY  - JOUR
AU  - Lorente-Herraiz, Laura
AU  - Cuesta Martínez, Ángel
AU  - Granado, Jaime
AU  - Recio-Poveda, Lucía
AU  - Botella, Luisa-María
AU  - Albiñana, Virginia
PY  - 2024
DO  - 10.3390/ijms25073952
SN  - 1422-0067
UR  - https://hdl.handle.net/20.500.14352/115589
T2  - Int. J. Mol. Sci
AB  - Cerebral cavernous malformation (CCM) or familial cavernomatosis is a rare, autosomal dominant, inherited disease characterized by the presence of vascular malformations consisting of blood vessels with an abnormal structure in the form of clusters....
LA  - eng
M2  - 3952
PB  - MDPI
KW  - cavernous malformations
KW  - cerebral cavernous malformation (CCM)
KW  - cavernomatosis
KW  - vascular malformations
KW  - primary endothelial cells
KW  - splicing
KW  - CCM signaling complex
KW  - Krit-1
TI  - Molecular and Cellular Characterization of Primary Endothelial Cells from a Familial Cavernomatosis Patient
TY  - journal article
VL  - 25
ER  -