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Novel variants of MEFV and NOD2 genes in familial hidradenitis suppurativa: A case report
We report a two-generation Canadian family of Armenian ancestry with hidradenitis suppurativa where novel mutations in MEVF and NOD2 genes were identified. The father and both children shared a mild-to-moderate hidradenitis suppurativa phenotype together with the features of follicular occlusion (e....
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| Yayımlandı: | SAGE Open Med Case Rep |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
SAGE Publications
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7522817/ https://ncbi.nlm.nih.gov/pubmed/33029352 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2050313X20953113 |
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