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Novel homozygous variants in PRORP expand the genotypic spectrum of combined oxidative phosphorylation deficiency 54 (2023)

First Author: Newman W

Attributed to: Pleiotropic disorders of mitochondrial translation funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.21203/rs.3.rs-2844536/v1

Publication URI: http://dx.doi.org/10.21203/rs.3.rs-2844536/v1

Type: Preprint