Unraveling the Molecular Determinants of a Rare Human Mitochondrial Disorder Caused by the P144L Mutation of Fdx2

AuthID
 P-017-AJM
7
Author(s)
Doni, D
·
Susini, B
·
Fonseca, BM
·
Louro, RO
·
Costantini, P
·
Ciofi-Baffoni, S
Tipo de Documento
Article
Year published
2024
Publicado
in PROTEIN SCIENCE, ISSN: 0961-8368
Volume: 33, Número: 11
Indexing
Wos®
Scopus®
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 39467201
SCOPUS: 2-s2.0-85207789424
Wos: WOS:001369121800001
Source Identifiers
ISSN: 0961-8368
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