FCDGC: Studying Variants of CAD Deficiency to Improve Diagnosis
17 ott 2023 ·
1 min. 23 sec.
Scarica e ascolta ovunque
Scarica i tuoi episodi preferiti e goditi l'ascolto, ovunque tu sia! Iscriviti o accedi ora per ascoltare offline.
Descrizione
New research from the Frontiers in Congenital Disorders of Glycosylation Consortium (FCDGC). This summary is based on a paper published in the Journal of Inherited Metabolic Disease on August 4,...
mostra di più
New research from the Frontiers in Congenital Disorders of Glycosylation Consortium (FCDGC). This summary is based on a paper published in the Journal of Inherited Metabolic Disease on August 4, 2023, titled "Beyond genetics: Deciphering the impact of missense variants in CAD deficiency."
Read the paper here: https://onlinelibrary.wiley.com/doi/10.1002/jimd.12667
Learn more about FCDGC: https://fcdgc.rarediseasesnetwork.org
mostra meno
Read the paper here: https://onlinelibrary.wiley.com/doi/10.1002/jimd.12667
Learn more about FCDGC: https://fcdgc.rarediseasesnetwork.org
Informazioni
| Autore | RDCRN |
| Organizzazione | RDCRN |
| Sito | - |
| Tag |
Copyright 2024 - Spreaker Inc. an iHeartMedia Company
Commenti