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                                       Details for article 60 of 70 found articles
 
 
  Selected AGXT gene mutations analysis provides a genetic diagnosis in 28% of Tunisian patients with primary hyperoxaluria
 
 
Title: Selected AGXT gene mutations analysis provides a genetic diagnosis in 28% of Tunisian patients with primary hyperoxaluria
Author: Mbarek, Ibtihel Benhaj
Abroug, Saoussen
Omezzine, Asma
Zellama, Dorsaf
Achour, Abdellatif
Harbi, Abdelaziz
Bouslama, Ali
Appeared in: BMC nephrology
Paging: Volume 12 (2011) nr. 1 pages xx
Year: 2011-05-25
Contents:
Publisher: BioMed Central, London
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

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