Unusual presentation of a five-month-old boy with NaPi2a homozygous mutation without hyperphosphaturia: Case report and review of the literature.
NaPi2a gene
SLC34A gene
case report
hypercalciuria
nephrocalcinosis
phosphaturia
Journal
Clinical case reports
ISSN: 2050-0904
Titre abrégé: Clin Case Rep
Pays: England
ID NLM: 101620385
Informations de publication
Date de publication:
Sep 2021
Sep 2021
Historique:
received:
07
03
2021
revised:
15
07
2021
accepted:
09
08
2021
entrez:
17
9
2021
pubmed:
18
9
2021
medline:
18
9
2021
Statut:
epublish
Résumé
Deletions of the
Identifiants
pubmed: 34532044
doi: 10.1002/ccr3.4740
pii: CCR34740
pmc: PMC8435227
doi:
Types de publication
Case Reports
Langues
eng
Pagination
e04740Informations de copyright
© 2021 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
Déclaration de conflit d'intérêts
All authors declare no conflict of interest.
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