Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformation-Reference-Cited by-同舟云学术

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

Published:2021-09-07 Issue:10 Volume:9 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Choksi Foram¹^ORCID,Weinsheimer Shantel²³^ORCID,Nelson Jeffrey²,Pawlikowska Ludmila²³^ORCID,Fox Christine K.⁴,Zafar Atif⁵,Mabray Marc C.⁶,Zabramski Joseph⁷,Akers Amy⁸,Hart Blaine L.⁶,Morrison Leslie⁵,McCulloch Charles E.¹,Kim Helen¹²³^ORCID

Affiliation:

1. Department of Epidemiology and Biostatistics University of California San Francisco San Francisco California USA

2. Department of Anesthesia and Perioperative Care Center for Cerebrovascular Research University of California San Francisco San Francisco California USA

3. Institute for Human Genetics University of California San Francisco San Francisco California USA

4. Department of Neurology University of California San Francisco San Francisco California USA

5. Department of Neurology University of New Mexico Albquerque New Mexico USA

6. Department of Radiology University of New Mexico Albquerque New Mexico USA

7. Department of Neurosurgery Barrow Neurological Institute Phoenix Arizona USA

8. Angioma Alliance Durham North Carolina USA

Funder

National Institutes of Health

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology