Author:
M’DIMEGH SAOUSSEN,AQUAVIVA-BOURDAIN CÉCILE,OMEZZINE ASMA,M’BAREK IBTIHEL,SOUCHE GENEVIÉVE,ZELLAMA DORSAF,ABIDI KAMEL,ACHOUR ABDELATTIF,GARGAH TAHAR,ABROUG SAOUSSEN,BOUSLAMA ALI
Publisher
Springer Science and Business Media LLC
Reference27 articles.
1. Amoroso A., Pirulli D., Florian F., Puzzer D., Boniotto M., Crovella S. et al. 2001 AGXT gene mutations and their influence on clinical heterogeneity of type 1 primary hyperoxaluria. J. Am. Soc. Nephrol. 12, 2072–2079.
2. Antonarakis S. E., Krawczak M. and Cooper D. N. 2001 The nature and mechanisms of human gene mutation. In: The metabolic and molecular bases of inherited disease, 8th edition, pp. 343–377.
3. Cochat P., Fargue S. and Harambat J. 2010 Primary hyperoxaluria type 1: strategy for organ transplantation. Curr. Opin. Organ Transplant. 15, 590–593.
4. Coulter-Mackie M. B., Lian Q., Applegarth D. and Toone J. 2005 The major allele of the alanine : glyoxylate aminotransferase gene: nine novel mutations and polymorphisms associated with primary hyperoxaluria type 1. Mol. Genet. Metab. 86, 172–178.
5. Danpure C. J. and Jennings P. R. 1986 Peroxisomal alanine: glyoxylate aminotransferase deficiency in primary hyperoxaluria type I. FEBS Lett. 201, 20–24.
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