FCDGC: Exploring the Neurological Characteristics of PMM2-Congenital Disorder of Glycosylation Using Human In Vitro Neural Models
24 apr 2024 ·
1 min. 49 sec.
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Descrizione
New research from the Frontiers in Congenital Disorders of Glycosylation Consortium (FCDGC). This summary is based on a paper published in the journal Cell Reports on March 1, 2024, titled...
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New research from the Frontiers in Congenital Disorders of Glycosylation Consortium (FCDGC). This summary is based on a paper published in the journal Cell Reports on March 1, 2024, titled "Neural and metabolic dysregulation in PMM2-deficient human in vitro neural models."
Read the paper here: https://www.cell.com/cell-reports/fulltext/S2211-1247(24)00211-0?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS2211124724002110%3Fshowall%3Dtrue
Learn more about FCDGC: https://fcdgc.rarediseasesnetwork.org
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Read the paper here: https://www.cell.com/cell-reports/fulltext/S2211-1247(24)00211-0?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS2211124724002110%3Fshowall%3Dtrue
Learn more about FCDGC: https://fcdgc.rarediseasesnetwork.org
Informazioni
| Autore | RDCRN |
| Organizzazione | RDCRN |
| Sito | - |
| Tag |
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