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P115: Identification of a novel SDHB c.638T>G, p.M213R likely pathogenic variant accountable for hereditary paraganglioma-pheochromocytoma syndrome: A case report
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Published in: | Genetics in Medicine Open 2024, Vol.2, p.100996, Article 100996 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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ISSN: | 2949-7744 2949-7744 |
DOI: | 10.1016/j.gimo.2024.100996 |