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A recurrent homozygous missense DPM3 variant leads to muscle and brain disease. (2022)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1111/cge.14208

PubMed Identifier: 35932216

Publication URI: http://europepmc.org/abstract/MED/35932216

Type: Journal Article/Review

Volume: 102

Parent Publication: Clinical genetics

Issue: 6

ISSN: 0009-9163