Detection of compound heterozygous variants in LPIN1 does not necessarily imply pathogenicity in a patient with rhabdomyolysis.
LPIN1
genetics
myoglobinurea
renal insufficiency
rhabdomyolysis
Journal
F1000Research
ISSN: 2046-1402
Titre abrégé: F1000Res
Pays: England
ID NLM: 101594320
Informations de publication
Date de publication:
2020
2020
Historique:
accepted:
07
01
2020
entrez:
11
9
2020
pubmed:
12
9
2020
medline:
30
10
2020
Statut:
epublish
Résumé
In a recent article by Yim
Identifiants
pubmed: 32913636
doi: 10.12688/f1000research.21589.1
pmc: PMC7429921
doi:
Substances chimiques
LPIN1 protein, human
EC 3.1.3.4
Phosphatidate Phosphatase
EC 3.1.3.4
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
15Informations de copyright
Copyright: © 2020 Finsterer J and Aliyev R.
Déclaration de conflit d'intérêts
No competing interests were disclosed.
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