A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi-Goutières and Singleton-Merten syndromes in a single patient.
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| Description | scientific article published on 5 August 2017 |
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| Publication date | December 22, 2017 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |