A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi–Goutières and Singleton–Merten syndromes in a single patient
T. Takeichi, C. Katayama, T. Tanaka, Y. Okuno, N. Murakami, M. Kono, K. Sugiura, Y. Aoyama, M. Akiyama
研究成果: ジャーナルへの寄稿 › Letter › 査読
16
被引用数
(Scopus)