Benutzer: Gast  Login
Weniger Felder
Einfache Suche
Titel:

Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders.

Dokumenttyp:
Article; Journal Article
Autor(en):
Kaiyrzhanov, Rauan; Rad, Aboulfazl; Lin, Sheng-Jia; Bertoli-Avella, Aida; Kallemeijn, Wouter W; Godwin, Annie; Zaki, Maha S; Huang, Kevin; Lau, Tracy; Petree, Cassidy; Efthymiou, Stephanie; Karimiani, Ehsan Ghayoor; Hempel, Maja; Normand, Elizabeth A; Rudnik-Schöneborn, Sabine; Schatz, Ulrich A; Baggelaar, Marc P; Ilyas, Muhammad; Sultan, Tipu; Alvi, Javeria Raza; Ganieva, Manizha; Fowler, Ben; Aanicai, Ruxandra; Tayfun, Gulsen Akay; Al Saman, Abdulaziz; Alswaid, Abdulrahman; Amiri, Nafise; Asil...     »
Abstract:
The acyl-CoA-binding domain-containing protein 6 (ACBD6) is ubiquitously expressed, plays a role in the acylation of lipids and proteins and regulates the N-myristoylation of proteins via N-myristoyltransferase enzymes (NMTs). However, its precise function in cells is still unclear, as is the consequence of ACBD6 defects on human pathophysiology. Using exome sequencing and extensive international data sharing efforts, we identified 45 affected individuals from 28 unrelated families (consanguinit...     »
Zeitschriftentitel:
Brain
Jahr:
2024
Band / Volume:
147
Heft / Issue:
4
Seitenangaben Beitrag:
1436-1456
Volltext / DOI:
doi:10.1093/brain/awad380
PubMed:
http://view.ncbi.nlm.nih.gov/pubmed/37951597
Print-ISSN:
0006-8950
TUM Einrichtung:
Institut für Humangenetik (Prof. Winkelmann)
 BibTeX