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

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Bibliographic Details
Published in:Journal of the neurological sciences 2020-01, Vol.408, p.116577, Article 116577
Main Authors: 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
Format: Article
Language:English
Subjects:
Adenosine Triphosphatases - genetics
Genetic Variation - genetics
Humans
Intracranial Arterial Diseases - diagnostic imaging
Intracranial Arterial Diseases - drug therapy
Intracranial Arterial Diseases - genetics
Intracranial arterial stenosis
Male
Middle Aged
Nilotinib
Protein-Tyrosine Kinases - antagonists & inhibitors
Protein-Tyrosine Kinases - metabolism
Pyrimidines - adverse effects
RNF213
Ubiquitin-Protein Ligases - genetics
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ISSN:0022-510X
1878-5883
DOI:10.1016/j.jns.2019.116577