Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis. (2021)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41431-021-00937-3

PubMed Identifier: 34267341

Publication URI: http://europepmc.org/abstract/MED/34267341

Type: Journal Article/Review

Volume: 29

Parent Publication: European journal of human genetics : EJHG

Issue: 9

ISSN: 1018-4813