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bibliographicCitation Hara S, Mukawa M, Akagawa H, Thamamongood T, Inaji M, Tanaka Y, Maehara T, Kasuya H, Nariai T. Absence of the RNF213 p.R4810K variant may indicate a severe form of pediatric moyamoya disease in Japanese patients. J Neurosurg Pediatr. 2022 Jan 01;29(1):48–56. doi: 10.3171/2021.7.peds21250. PMID: 34624841.
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title Absence of the RNF213 p.R4810K variant may indicate a severe form of pediatric moyamoya disease in Japanese patients
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