Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia
Vaz, McDermott et al. identify variants in PCYT2, which encodes a key gene in phospholipid biosynthesis, in five individuals with a new complex hereditary spast
Gespeichert in:
| Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , , , |
|---|---|
| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2019
|
| In: |
Brain
Year: 2019, Jahrgang: 142, Heft: 11, Pages: 3382-3397 |
| ISSN: | 1460-2156 |
| DOI: | 10.1093/brain/awz291 |
| Online-Zugang: | Verlag, kostenfrei, Volltext: https://doi.org/10.1093/brain/awz291 Verlag, kostenfrei, Volltext: https://academic.oup.com/brain/article/142/11/3382/5601846 |
| Verfasserangaben: | Frédéric M. Vaz, John H. McDermott, Mariëlle Alders, Saskia B. Wortmann, Stefan Kölker, Mia L. Pras-Raves, Martin A. T. Vervaart, Henk van Lenthe, Angela C. M. Luyf, Hyung L. Elfrink, Kay Metcalfe, Sara Cuvertino, Peter E. Clayton, Rebecca Yarwood, Martin P. Lowe, Simon Lovell, Richard C. Rogers, Antoine H. C. van Kampen, Jos P. N. Ruiter, Ronald J. A. Wanders, Sacha Ferdinandusse, Michel van Weeghel, Marc Engelen, Siddharth Banka |
| Zusammenfassung: | Vaz, McDermott et al. identify variants in PCYT2, which encodes a key gene in phospholipid biosynthesis, in five individuals with a new complex hereditary spast |
|---|---|
| Beschreibung: | Gesehen am 24.04.2020 |
| Beschreibung: | Online Resource |
| ISSN: | 1460-2156 |
| DOI: | 10.1093/brain/awz291 |