Association of hereditary angioedema type 1 with developmental anomalies due to a large and unusual de novo pericentromeric rearrangement of chromosome 11 spanning the entire C1 inhibitor gene (SERPING1)
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| Description | article |
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author: Athina L Van Gasse Frank Kooy Didier G Ebo Vito Sabato Bettina Blaumeiser |
| Publication date | October 16, 2018 |
| Language | English |
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