Search Results - Valenti, V.

  • Showing 1 - 1 results of 1
Refine Results
  1. 1
    Homozygous familial hypobetalipoproteinemia: Two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature

    Homozygous familial hypobetalipoproteinemia: Two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature by Cefalù, A., Norata, Giuseppe, Ghiglioni, D., Noto, D., Uboldi, P., Garlaschelli, K., Baragetti, A., Spina, R., Valenti, V., Pederiva, C., Riva, E., Terracciano, L., Zoja, A., Grigore, L., Averna, M., Catapano, A.

    Published 2015
    Get full text

Search Tools: