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
Author Information: Departments of Dermatology
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