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WNK1/HSN2 isoform and the regulation of KCC2 activity
Hereditary sensory and autonomic neuropathy type 2 is a rare autosomal recessive pathology presenting with early onset peripheral sensory defects. It arises from mutations affecting a specific isoform of the WNK1 kinase (with-no-lysine protein kinase 1) termed WNK1/HSN2. The role of WNK1 in the nerv...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Landes Bioscience
2013
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3933052/ https://ncbi.nlm.nih.gov/pubmed/25003007 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/rdis.26537 |
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