Search

Search Constraints

You searched for: Author/Creator Aoyama, Y.

Search Results

3. A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi–Goutières and Singleton–Merten syndromes in a single patient. (1st February 2018)

4. A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi–Goutières and Singleton–Merten syndromes in a single patient. (22nd December 2017)