Novel compound heterozygous ATP1A2 variants in a patient with fetal akinesia/hypokinesia sequence.
ATP1A2
fetal akinesia/hypokinesia sequence
Journal
American journal of medical genetics. Part A
ISSN: 1552-4833
Titre abrégé: Am J Med Genet A
Pays: United States
ID NLM: 101235741
Informations de publication
Date de publication:
23 Oct 2023
23 Oct 2023
Historique:
revised:
10
10
2023
received:
31
07
2023
accepted:
12
10
2023
medline:
23
10
2023
pubmed:
23
10
2023
entrez:
23
10
2023
Statut:
aheadofprint
Résumé
ATP1A2 encodes a subunit of sodium/potassium-transporting adenosine triphosphatase (Na
Identifiants
pubmed: 37870493
doi: 10.1002/ajmg.a.63453
doi:
Types de publication
Case Reports
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : HUSM Grant-in-Aid from Hamamatsu University School of Medicine
Organisme : Japan Agency for Medical Research and Development
ID : JP23ek0109549
Organisme : Japan Agency for Medical Research and Development
ID : JP23ek01099674
Organisme : Japan Agency for Medical Research and Development
ID : JP23ek0109637
Organisme : Japan Society for the Promotion of Science
ID : JP 20H03641
Organisme : Japan Society for the Promotion of Science
ID : JP23H02875
Organisme : Japan Society for the Promotion of Science
ID : JP20K08236
Organisme : Japan Society for the Promotion of Science
ID : JP21K06819
Organisme : Takeda Science Foundation
Informations de copyright
© 2023 Wiley Periodicals LLC.
Références
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