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                                       Details for article 31 of 32 found articles
 
 
  Unveiling atypical diagnoses: when whole-genome analysis performed for refractory infantile hypomagnesemia reveals primary hyperoxaluria
 
 
Title: Unveiling atypical diagnoses: when whole-genome analysis performed for refractory infantile hypomagnesemia reveals primary hyperoxaluria
Author: Kayal, Dima
Vedrine, Enzo
Goursaud, Claire
Sellier-Leclerc, Anne-Laure
Acquaviva-Bourdain, Cécile
Bertholet-Thomas, Aurelia
Bacchetta, Justine
Appeared in: Pediatric nephrology
Paging: Volume 40 () nr. 1 pages 85-87
Year: 2024-08-01
Contents:
Publisher: Springer Berlin Heidelberg, Berlin/Heidelberg
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 31 of 32 found articles
 
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