FCDGC: Exploring the Role of NGLY1 Deficiency in Patients with NGLY1-Congenital Disorder of Deglycosylation
Descarga y escucha en cualquier lugar
Descarga tus episodios favoritos y disfrútalos, ¡dondequiera que estés! Regístrate o inicia sesión ahora para acceder a la escucha sin conexión.
7 de nov. de 2022 ·
1m 46s
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 September 14,...
mostra más
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 September 14, 2022, titled "N-glycoproteomics reveals distinct glycosylation alterations in NGLY1-deficient patient-derived dermal fibroblasts."
Read the paper here: https://onlinelibrary.wiley.com/doi/10.1002/jimd.12557
Learn more about FCDGC: https://www.rarediseasesnetwork.org/fcdgc
mostra menos
Read the paper here: https://onlinelibrary.wiley.com/doi/10.1002/jimd.12557
Learn more about FCDGC: https://www.rarediseasesnetwork.org/fcdgc
Información
| Autor | RDCRN |
| Página web | - |
| Etiquetas |
Copyright 2024 - Spreaker Inc. an iHeartMedia Company
