Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome.

ATIK T., KOPARIR A. , BADEMCI G., FOSTER J. 2. , Altunoglu U. , MUTLU G., ...More

Orphanet journal of rare diseases, vol.10, pp.128, 2015 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 10
  • Publication Date: 2015
  • Doi Number: 10.1186/s13023-015-0345-3
  • Title of Journal : Orphanet journal of rare diseases
  • Page Numbers: pp.128