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The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype. (2021)

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