Variable Presentation of Primary Hyperoxaluria Type 1 in 2 Patients Homozygous for a Novel Combined Deletion and Insertion Mutation inExon 8 of the AGXT Gene

Publisher： Karger

E-ISSN： 2235-3186|78|4|485-488

ISSN： 1660-8151

Source： Nephron, Vol.78, Iss.4, 1998-03, pp. : 485-488

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Primary Hyperoxaluria Type 1 in Japan

By  

American Journal of Nephrology, Vol. 25, Iss. 3, 2005-07 ,pp. : 297-302

Karger

Access to resources Recommend Favorite

Assessment of Urine Proteomics in Type 1 Primary Hyperoxaluria

By  

American Journal of Nephrology, Vol. 43, Iss. 4, 2016-05 ,pp. : 293-303

Karger

Access to resources Recommend Favorite

Preliminary Evidence for Ethnic Differences in Primary Hyperoxaluria Type 1 Genotype

By  

American Journal of Nephrology, Vol. 25, Iss. 3, 2005-07 ,pp. : 264-268

Karger

Access to resources Recommend Favorite

Molecular Etiology of Primary Hyperoxaluria Type 1: New Directions for Treatment

By  

American Journal of Nephrology, Vol. 25, Iss. 3, 2005-07 ,pp. : 303-310

Karger

Access to resources Recommend Favorite

A Novel Homozygous SLC2A9 Mutation Associated with Renal-Induced Hypouricemia

By  

American Journal of Nephrology, Vol. 43, Iss. 4, 2016-04 ,pp. : 245-250

Karger

Access to resources Recommend Favorite