Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformation,Molecular Genetics & Genomic Medicine

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Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformation
Molecular Genetics & Genomic Medicine ( IF 1.5 ) Pub Date : 2021-09-07 , DOI: 10.1002/mgg3.1794
Foram Choksi ₁ , Shantel Weinsheimer _{2,

3} , Jeffrey Nelson ₂ , Ludmila Pawlikowska _{2,

3} , Christine K Fox ₄ , Atif Zafar ₅ , Marc C Mabray ₆ , Joseph Zabramski ₇ , Amy Akers ₈ , Blaine L Hart ₆ , Leslie Morrison ₅ , Charles E McCulloch ₁ , Helen Kim _{1,

2,

3}

Affiliation

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.

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