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A Novel Homozygous Founder Variant of RTN4IP1 in Two Consanguineous Saudi Families. (2022)

First Author: Aldosary M

Attributed to: Pleiotropic disorders of mitochondrial translation funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.3390/cells11193154

PubMed Identifier: 36231115

Publication URI: http://europepmc.org/abstract/MED/36231115

Type: Journal Article/Review

Volume: 11

Parent Publication: Cells

Issue: 19

ISSN: 2073-4409