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A unique missense mutation in the RING domain impairs MID1 E3 ubiquitin ligase activity and localisation and is associated with uncommon Opitz Syndrome-like signs.

Authors :
Mascaro M
D'Ambrosio L
Lazzari E
Almoguera B
Swafiri ST
Zanchetta ME
Meroni G
Source :
Biochimica et biophysica acta. Molecular basis of disease [Biochim Biophys Acta Mol Basis Dis] 2024 Apr; Vol. 1870 (4), pp. 167126. Date of Electronic Publication: 2024 Mar 18.
Publication Year :
2024

Abstract

Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Details

Language :
English
ISSN :
1879-260X
Volume :
1870
Issue :
4
Database :
MEDLINE
Journal :
Biochimica et biophysica acta. Molecular basis of disease
Publication Type :
Academic Journal
Accession number :
38508475
Full Text :
https://doi.org/10.1016/j.bbadis.2024.167126