Literature DB >> 13559890

Observations on the possible genetic basis of primary hyperoxaluria.

H E ARCHER, A E DORMER, E F SCOWEN, R W WATTS.   

Abstract

Entities:  

Keywords:  OXALATES/in urine

Mesh：

Substances：

Year:  1958        PMID： 13559890     DOI： 10.1111/j.1469-1809.1958.tb01432.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN： 0003-4800            Impact factor:   1.670


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  3 in total

Review 1.  INHERITED ENZYME DEFECTS: A REVIEW.

Authors:  T HARGREAVES
Journal:  J Clin Pathol       Date:  1963-07       Impact factor: 3.411

2.  [Oxalosis. Part I. Empirical studies].

Authors:  F LARGIADER; H U ZOLLINGER
Journal:  Virchows Arch Pathol Anat Physiol Klin Med       Date:  1960

Review 3.  Recent advances in the understanding, diagnosis and treatment of primary hyperoxaluria type 1.

Authors:  C J Danpure
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982
  3 in total

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