Congenital disorder of glycosylation type Id (CDG Id): phenotypic, biochemical and molecular characterization of a new patient
- Rimella-Le-Huu, A. et al
- swissbib.ch:(NATIONALLICENCE)springer-10.1007/s10545-008-0959-x
Main file(s):
![]() |
|||||||
version 1 |
|