檢索結果 - Fabio Maset

  • Showing 1 - 1 results of 1
Refine Results
  1. 1
    Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I

    Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I 由 Barbara Cellini, Riccardo Montioli, Alessandro Paiardini, Antonio Lorenzetto, Fabio Maset, Tiziana Bellini, Elisa Oppici, Carla Borri Voltattorni

    出版 2010
    獲取全文
    Artigo
    加到收藏夾
    Saved in:

檢索工具: