Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders. (2023)

First Author: Kaiyrzhanov R
Attributed to:  Molecular and bioinformatic resources for research using Xenopus funded by BBSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awad380

PubMed Identifier: 37951597

Publication URI: http://europepmc.org/abstract/MED/37951597

Type: Journal Article/Review

Parent Publication: Brain : a journal of neurology

ISSN: 0006-8950