| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8681869 | Clinical Neurology and Neurosurgery | 2018 | 14 Pages |
Abstract
Collectively, we present a unique case of A-MMS with genetic variant of RNF213 p.R4810K and p.T1727M, manifesting as progression. Based on the family tree, these two mutations are on the same RNF213 haplotype. Whether atherosclerosis is the cause of A-MMS or it further exacerbates the injury of MMD to the A-MMS patients with RNF213 gene variant is a question to be investigated.
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Authors
Ying Liu, Xueying Wu, Zhaoyang Fan, Jingdan Cheng, Lele Zhong, Yongzhong Lin, Xiaofeng Qu,