Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study (2024)

First Author: Bisschoff M
Attributed to:  Pleiotropic disorders of mitochondrial translation funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1186/s13023-023-03014-8

PubMed Identifier: 38221620

Publication URI: http://europepmc.org/abstract/MED/38221620

Type: Journal Article/Review

Parent Publication: Orphanet Journal of Rare Diseases

Issue: 1

ISSN: 1750-1172