The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype. (2021)
Attributed to:
MRC Strategic Award to establish an International Centre for Genomic Medicine in Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1007/s00109-021-02124-9
PubMed Identifier: 34536092
Publication URI: http://europepmc.org/abstract/MED/34536092
Type: Journal Article/Review
Volume: 99
Parent Publication: Journal of molecular medicine (Berlin, Germany)
Issue: 12
ISSN: 0946-2716