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
18
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(Scopus)