Comparative proteomics reveals deficiency of SLC9A1 (sodium/hydrogen exchanger NHE1) in β-adducin null red cells

Spherocytosis is one of the most common inherited disorders, yet presents with a wide range of clinical severity. While several genes have been found mutated in patients with spherocytosis, the molecular basis for the variability in severity of haemolytic anaemia is not entirely understood. To ident...

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Bibliographic Details
Published in:Br J Haematol
Main Authors: Wooden, Jason M., Finney, Greg L., Rynes, Eric, MacCoss, Michael J., Lambert, Amy J., Robledo, Raymond F., Peters, Luanne L., Gilligan, Diana M.
Format: Artigo
Language:Inglês
Published: 2011
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Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4515348/
https://ncbi.nlm.nih.gov/pubmed/21689084
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2141.2011.08612.x
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