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Paper Report for: Stefanutti_2013_Atheroscler.Suppl_14_73

Reference

Title: A three month-old infant with severe hyperchylomicronemia: Molecular diagnosis and extracorporeal treatment
Stefanutti C, Gozzer M, Pisciotta L, D'Eufemia P, Bosco G, Morozzi C, Papadia F, Shafii M, Di Giacomo S, Bertolini S
Ref: Atheroscler Suppl, 14:73, 2013 : PubMed

        



Related information

Gene_Locus| human-LPL
Mutation | G81D_human-LPL,



Citations formats

Stefanutti C, Gozzer M, Pisciotta L, D'Eufemia P, Bosco G, Morozzi C, Papadia F, Shafii M, Di Giacomo S, Bertolini S (2013)
A three month-old infant with severe hyperchylomicronemia: Molecular diagnosis and extracorporeal treatment
Atheroscler Suppl 14: 73-6

Stefanutti C, Gozzer M, Pisciotta L, D'Eufemia P, Bosco G, Morozzi C, Papadia F, Shafii M, Di Giacomo S, Bertolini S (2013)
Atheroscler Suppl 14: 73-6



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