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 language | English (US) |
|---|---|
| Pages (from-to) | 274-278 |
| Number of pages | 5 |
| Journal | Annals of Clinical and Laboratory Science |
| Volume | 11 |
| Issue number | 3 |
| State | Published - 1981 |
ASJC Scopus subject areas
- Microbiology
- Immunology and Allergy
- Pathology and Forensic Medicine
- Immunology
- Molecular Biology
- Hematology
- Clinical Biochemistry
- Medical Laboratory Technology