Inherited disorders of amino acid transport in relation to the kidney

B. A. Buehler

Research output: Contribution to journalReview article

4 Scopus citations

Abstract

Cystinuria was first described in 1810. Since the initial description, a group of renal cellular transport deficit diseases has been characterized. The study of genetic dieases that create a specific aminoaciduria has expanded our knowledge of cellular structure, cellular transport, and intracellular concentration gradients. A review of the thories and experimental data obtained through investigations of renal aminoacidurias are presented.

Original languageEnglish (US)
Pages (from-to)274-278
Number of pages5
JournalAnnals of Clinical and Laboratory Science
Volume11
Issue number3
Publication statusPublished - Jan 1 1981

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ASJC Scopus subject areas

  • Microbiology
  • Immunology and Allergy
  • Pathology and Forensic Medicine
  • Immunology
  • Molecular Biology
  • Hematology
  • Clinical Biochemistry
  • Medical Laboratory Technology

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