Back to Search Start Over

TFP/LCHAD Deficiency Due to HADHA Gene Mutation.

Authors :
Chen QL
Zhang CM
Source :
Clinical pediatrics [Clin Pediatr (Phila)] 2024 Nov; Vol. 63 (11), pp. 1604-1607. Date of Electronic Publication: 2024 Feb 20.
Publication Year :
2024

Abstract

Competing Interests: Declaration of Conflicting InterestsThe author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Subjects

Subjects :
Humans
Infant
Lipid Metabolism, Inborn Errors genetics
Cardiomyopathies genetics
Nervous System Diseases genetics
Rhabdomyolysis genetics
Mutation
Mitochondrial Trifunctional Protein, alpha Subunit genetics
Mitochondrial Myopathies genetics

Details

Language :
English
ISSN :
1938-2707
Volume :
63
Issue :
11
Database :
MEDLINE
Journal :
Clinical pediatrics
Publication Type :
Academic Journal
Accession number :
38379183
Full Text :
https://doi.org/10.1177/00099228241233099
Full Text Access
View/download PDF

Tools

Authors Abstract Subjects Details