Molecular and Clinical Heterogeneity in Primary Hyperoxaluria Type 1-Reference-Cited by-同舟云学术

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Molecular and Clinical Heterogeneity in Primary Hyperoxaluria Type 1

Published:1991-04 Issue:4 Volume:17 Page:366-369
ISSN:0272-6386
Container-title:American Journal of Kidney Diseases
language:en
Short-container-title:American Journal of Kidney Diseases

Author:

Danpure Christopher J.

Publisher

Elsevier BV

Subject

Nephrology

Reference11 articles.

1. Primary hyperoxaluria;Williams,1983

2. Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type 1;Danpure;FEBS Lett,1986

3. Recent advances in the understanding, diagnosis and treatment of primary hyperoxaluria type 1;Danpure;J Inher Metab Dis,1989

4. Enzymological characterization of a feline analogue of primary hyperoxaluria type 2: A model for the human disease;Danpure;J Inherited Metab Dis,1989

5. Immunocytochemical localization of human hepatic alanine:glyoxylate aminotransferase in control subjects and patients with primary hyperoxaluria type l;Cooper;J Histochem Cytochem,1988

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