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‘Silent’ carriage of two familial Mediterranean fever gene mutations in large families with only a single identified patient

✍ Scribed by D Camus; Y Shinar; S Aamar; P Langevitz; I Ben-Zvi; A Livneh; M Lidar


Book ID
117948286
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
508 KB
Volume
82
Category
Article
ISSN
0009-9163

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Mutations in theMEFV gene in a large ser
✍ Dod�, C.; P�cheux, C.; Cazeneuve, C.; Cattan, D.; Dervichian, M.; Goossens, M.; 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 37 KB 👁 2 views

Familial Mediterranean fever (FMF) is an autosomal recessively inherited disease affecting patients of the Mediterranean basin. FMF is characterized by recurrent episodes of fever accompanied with topical signs of inflammation. Some patients can develop a renal amyloidosis associated (AA) amyloidosi