Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformation

Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformation

Abstract Background To investigate whether common variants in EPHB4 and RASA1 are associated with cerebral cavernous malformation (CCM) disease severity phenotypes, including intracranial hemorrhage (ICH), total and large lesion counts. Methods Familial CCM cases enrolled in the Brain Vascular Malfo...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Foram Choksi, Shantel Weinsheimer, Jeffrey Nelson, Ludmila Pawlikowska, Christine K. Fox, Atif Zafar, Marc C. Mabray, Joseph Zabramski, Amy Akers, Blaine L. Hart, Leslie Morrison, Charles E. McCulloch, Helen Kim
Formato: article
Lenguaje:EN
Publicado: Wiley 2021
Materias:
cerebral cavernous malformation
EPHB4
Ras‐Erk/Ras‐MAPK signaling
RASA1
vascular malformation
Genetics
QH426-470
Acceso en línea:https://doaj.org/article/9f363bcd55e644af80ceef59a0f22455
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Internet

https://doaj.org/article/9f363bcd55e644af80ceef59a0f22455

Ejemplares similares