A Homozygous NDUFS6 Variant Associated with Neuropathy and Optic Atrophy. (2024)
Attributed to:
Exosomal protein deficiencies: how abnormal RNA metabolism results in childhood-onset neurological diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.3233/jnd-230181
PubMed Identifier: 38217609
Publication URI: http://europepmc.org/abstract/MED/38217609
Type: Journal Article/Review
Parent Publication: Journal of neuromuscular diseases