RNF213 in moyamoya disease: Genotype–phenotype association and the underlying mechanism
Abstract. Moyamoya disease (MMD) is a cerebrovascular disorder characterized by a steno-occlusive internal carotid artery and compensatory vascular network formation. Although the precise pathogenic mechanism remains elusive, genetic association studies have identified RNF213 as the principal suscep...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Wolters Kluwer
2024-11-01
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| Cyfres: | Chinese Medical Journal |
| Mynediad Ar-lein: | http://journals.lww.com/10.1097/CM9.0000000000002985 |
| Tagiau: |
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!
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