A new genetic variant of hereditary apolipoprotein A-I amyloidosis: a case-report followed by discussion of diagnostic challenges and therapeutic options

• প্রধান লেখক: Myrto Moutafi (লেখক), Dimitrios C. Ziogas (লেখক), Spyros Michopoulos (লেখক), Tina Bagratuni (লেখক), Vassiliki Vasileiou (লেখক), Laura Verga (লেখক), Giampaolo Merlini (লেখক), Giovanni Palladini (লেখক), Charis Matsouka (লেখক), Meletios A. Dimopoulos (লেখক), Efstathios Kastritis (লেখক)
• বিন্যাস: গ্রন্থ
• প্রকাশিত: BMC, 2019-01-01T00:00:00Z.
• বিষয়গুলি: article
• অনলাইন ব্যবহার করুন: Connect to this object online.

Abstract Background Hereditary amyloidosis refers to a wide spectrum of rare diseases with different causative mutations in the genes of various proteins including transthyretin, apolipoprotein AI and AII, gelsolin, lysozyme, cystatin C, fibrinogen Aα-chain, β2-microglobulin, apolipoprotein CII and...