Barth Syndrome Cardiomyopathy: An Update.
Barth syndrome
TAFAZZIN
cardiolipin
cardiomyopathy
Journal
Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097
Informations de publication
Date de publication:
08 04 2022
08 04 2022
Historique:
received:
07
03
2022
revised:
23
03
2022
accepted:
02
04
2022
entrez:
23
4
2022
pubmed:
24
4
2022
medline:
27
4
2022
Statut:
epublish
Résumé
Barth syndrome (BTHS) is an X-linked mitochondrial lipid disorder caused by mutations in the
Identifiants
pubmed: 35456462
pii: genes13040656
doi: 10.3390/genes13040656
pmc: PMC9030331
pii:
doi:
Substances chimiques
Transcription Factors
0
Acyltransferases
EC 2.3.-
Types de publication
Journal Article
Review
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NHLBI NIH HHS
ID : R01 HL158761
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL157115
Pays : United States
Organisme : NHLBI NIH HHS
ID : R00 HL143210
Pays : United States
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