Considerations about the molecular basis of some kidney tubule disorders in relation to inbreeding and population displacement

Nefrologia (Engl Ed). 2020 Mar-Apr;40(2):126-132. doi: 10.1016/j.nefro.2019.08.004. Epub 2019 Nov 27.
[Article in English, Spanish]
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Acidosis, Renal Tubular / genetics
  • Anion Exchange Protein 1, Erythrocyte / genetics
  • Bartter Syndrome / genetics
  • Child
  • Claudins / genetics
  • Consanguinity*
  • Emigration and Immigration*
  • Gitelman Syndrome / ethnology
  • Gitelman Syndrome / genetics
  • Humans
  • Hypercalciuria / genetics
  • Hyperoxaluria / epidemiology
  • Hyperoxaluria / genetics
  • Kidney Calculi / genetics
  • Kidney Diseases / genetics*
  • Kidney Tubules*
  • Nephrocalcinosis / genetics
  • Renal Tubular Transport, Inborn Errors / genetics
  • Risk Factors
  • Roma / genetics
  • Spain / epidemiology
  • Urinary Calculi / genetics

Substances

  • Anion Exchange Protein 1, Erythrocyte
  • CLDN19 protein, human
  • Claudins
  • SLC4A1 protein, human
  • claudin 16

Supplementary concepts

  • Hypomagnesemia primary
  • Renal hypouricemia