Birt–Hogg–Dubé syndrome: a case report and a review of the literature

Background: Birt-Hogg-Dubé syndrome (BHDS) is a rare autosomal dominant inherited syndrome caused by mutations in the folliculin coding gene (FLCN). The clinical manifestations of the syndrome involve the skin, lungs, and kidneys. Because of the rarity of the syndrome, guidelines for diagnosis and m...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Eur Clin Respir J
Asıl Yazarlar: Jensen, Dea Kejlberg, Villumsen, Anders, Skytte, Anne-Bine, Madsen, Mia Gebauer, Sommerlund, Mette, Bendstrup, Elisabeth
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Taylor & Francis 2017
Konular:
Review Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5345590/
https://ncbi.nlm.nih.gov/pubmed/28326182
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/20018525.2017.1292378
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