Immunohistochemical comparison of a case of inherited distal renal tubular acidosis (with a unique AE1 mutation) with an acquired case secondary to autoimmune disease

Nephrol Dial Transplant. 2007 Mar;22(3):807-12. doi: 10.1093/ndt/gfl662. Epub 2007 Jan 5.

Authors

Stephen Walsh¹, Clare M Turner, Ashley Toye, Carsten Wagner, Philippe Jaeger, Christopher Laing, Robert Unwin

Affiliation

¹ Department of Physiology, Royal Free and University College Medical School, Rowland Hill Street, London, UK. [email protected]

PMID: 17205967
DOI: 10.1093/ndt/gfl662

No abstract available

Publication types

Case Reports

MeSH terms

Acidosis, Renal Tubular / complications
Acidosis, Renal Tubular / genetics
Acidosis, Renal Tubular / metabolism*
Adult
Aged
Anion Exchange Protein 1, Erythrocyte / genetics*
Anion Exchange Protein 1, Erythrocyte / metabolism
Bicarbonates / metabolism
DNA / genetics
Erythrocytes / metabolism
Female
Gene Expression*
Genetic Predisposition to Disease
Humans
Immunohistochemistry
Male
Mutation*
Proton-Translocating ATPases / metabolism
Sjogren's Syndrome / complications
Sjogren's Syndrome / genetics
Sjogren's Syndrome / metabolism*

Substances

Anion Exchange Protein 1, Erythrocyte
Bicarbonates
SLC4A1 protein, human
DNA
Proton-Translocating ATPases