Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformation.
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DOI: 10.1002/mgg3.1794
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… read more here.
Keywords: malformation; severity; variants ephb4; cerebral cavernous ... See more keywords