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The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20 |
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| Authors: | Caprioli J Bettinaglio P Zipfel P F Amadei B Daina E Gamba S Skerka C Marziliano N Remuzzi G Noris M;Itaslian Registry of Familial and Recurrent HUS/TTP |
| Institution: | Clinical Research Center for Rare Diseases, Aldo e Cele Daccò, Mario Negri Institute for Pharmacological Research, Via Gavazzeni, 11, 24125 Bergamo, Italy. caprioli@marionegri.it |
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| 本文献已被 PubMed 等数据库收录！ | |