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Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data. (2021)

First Author: Matalonga L

Attributed to: Disease mechanisms and therapy for inherited disorders of the neuromuscular synapse. funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41431-021-00934-6

PubMed Identifier: 34393220

Publication URI: http://europepmc.org/abstract/MED/34393220

Type: Journal Article/Review

Volume: 29

Parent Publication: European journal of human genetics : EJHG

Issue: 9

ISSN: 1018-4813