📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

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

Volume: 19

Parent Publication: Orphanet journal of rare diseases

Issue: 1

ISSN: 1750-1172