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

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 Malformation...

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Detalles Bibliográficos
Autores principales: Choksi, Foram, Weinsheimer, Shantel, Nelson, Jeffrey, Pawlikowska, Ludmila, Fox, Christine K., Zafar, Atif, Mabray, Marc C., Zabramski, Joseph, Akers, Amy, Hart, Blaine L., Morrison, Leslie, McCulloch, Charles E., Kim, Helen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580075/
https://www.ncbi.nlm.nih.gov/pubmed/34491620
http://dx.doi.org/10.1002/mgg3.1794

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