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Article

Role of RNF213 p.4810K variant in the development of intracranial arterial disease in patients treated with nilotinib.

Journal of the neurological sciences - 15 Jan 2020

Uemura Masahiro, Kanazawa Masato, Yamagishi Takuma, Nagai Takahiro, Takahashi Mami, Koide Shingo, Tada Masayoshi, Shimbo Junsuke, Isami Aiko, Makino Kunihiko, Masuko Masayoshi, Nikkuni Kouji, Okamoto Kouichirou, Igarashi Shuichi, Morita Kenichi, Onodera Osamu

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PMID: 31733606
DOI: 10.1016/j.jns.2019.116577

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Role of RNF213 p.4810K variant in the development of intracranial arterial disease in patients treated with nilotinib.PMID 31733606Read ↗

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Development of atherosclerotic-moyamoya syndrome with genetic variant of RNF213 p.R4810K and p.T1727M: A case report.Semantic proximity Read ↗

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