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Arteriovenous Malformation Phenotype Resembling Congenital Hemangioma Contains KRAS Mutations
Extracranial arteriovenous malformation (AVM) is most commonly caused by a somatic mutation in MAP2K1. We report two patients with vascular anomalies that had an unclear clinical diagnosis most consistent with either an AVM or congenital hemangioma. Lesions were cutaneous, reddish-purple with telang...
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| Yayımlandı: | Clin Genet |
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| Asıl Yazarlar: | , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7955771/ https://ncbi.nlm.nih.gov/pubmed/32799314 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cge.13833 |
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