Search Results - Isabelle Chantret

  • Showing 1 - 1 results of 1
Refine Results
  1. 1

    An ALG12-CDG patient with a novel homozygous intronic mutation associated with low ALG12 mRNA by Sandrine Vuillaumier-Barrot, Thierry Dupré, Tiffany Andriantsihoarana, Vincent Desportes, David Cheillan, Stuart E. H. Moore, Isabelle Chantret

    Published in Orphanet Journal of Rare Diseases (2025-02-01)
    Get full text
    Article


Search Tools: