The rare A1 allele of the RNF213 p.R4810K variant may be associated with rapid progression of unilateral Moyamoya disease.
Answers are grounded in this paper and cite their sources.
May link RNF213 variant to Moyamoya progression in one family; hypothesis-generating and should not change practice.
No abstract yet. The journal hasn't published one we can show.
No takes yet. Share an insight, caveat, or question.
Mineharu et al. (2013) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: