HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients-Reference-Cited by-同舟云学术

HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients

Published:2016-08-26 Issue:3 Volume:31 Page:e22053
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J. Clin. Lab. Anal.

Author:

M'dimegh Saoussen¹,Aquaviva-bourdain Cécile²,Omezzine Asma¹,Souche Geneviéve²,M'barek Ibtihel¹,Abidi Kamel³,Gargah Tahar³,Abroug Saoussen⁴,Bouslama Ali¹

Affiliation:

1. Biochemistry Department; LR12SP11; Sahloul University Hospital; Sousse Tunisia

2. Laboratory of Inborn Metabolic Diseases; Centre de Biologie Est; Hospices Civils de Lyon; Lyon Bron Cedex France

3. Pediatric Department; Charles Nicolle University Hospital; Tunis Tunisia

4. Pediatric Department; LR12SP11; Sahloul University Hospital; Sousse Tunisia

Funder

Tunisian Ministry of Public Health

Ministry of Higher Education and Scientific Research

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry, medical,Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Reference16 articles.

1. Primary hyperoxaluria;Cochat;N Engl J Med,2013

2. Primary hyperoxaluria;Harambat;Int J Nephrol,2011

3. Primary hyperoxaluria type 1: Still challenging!;Cochat;Pediatr Nephrol,2006

4. Unusual painful sclerotic plaques on the legs of a patient with late diagnosis of primary hyperoxaluria type I;Herrmann;Br J Dermatol,2004

5. An update on primary hyperoxaluria;Hoppe;Nat Rev Nephrol,2012

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