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]
Affiliations
- 1 Sección de Nefrología Pediátrica, Hospital Universitario Nuestra Señora de Candelaria, Santa Cruz de Tenerife, España. Electronic address: vgarcianieto@gmail.com.
- 2 Unidad de Investigación, Hospital Universitario Nuestra Señora de Candelaria, Santa Cruz de Tenerife, España.
- 3 Sección de Nefrología Pediátrica, Hospital Universitario Nuestra Señora de Candelaria, Santa Cruz de Tenerife, España.
No abstract available
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Acidosis, Renal Tubular / genetics
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Anion Exchange Protein 1, Erythrocyte / genetics
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Bartter Syndrome / genetics
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Child
-
Claudins / genetics
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Consanguinity*
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Emigration and Immigration*
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Gitelman Syndrome / ethnology
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Gitelman Syndrome / genetics
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Humans
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Hypercalciuria / genetics
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Hyperoxaluria / epidemiology
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Hyperoxaluria / genetics
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Kidney Calculi / genetics
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Kidney Diseases / genetics*
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Kidney Tubules*
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Nephrocalcinosis / genetics
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Renal Tubular Transport, Inborn Errors / genetics
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Risk Factors
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Roma / genetics
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Spain / epidemiology
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Urinary Calculi / genetics
Substances
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Anion Exchange Protein 1, Erythrocyte
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CLDN19 protein, human
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Claudins
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SLC4A1 protein, human
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claudin 16
Supplementary concepts
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Hypomagnesemia primary
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Renal hypouricemia