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Functional analysis of human Na(+)/K(+)-ATPase familial or sporadic hemiplegic migraine mutations expressed in Xenopus oocytes

AIM: Functional characterization of ATP1A2 mutations that are related to familial or sporadic hemiplegic migraine (FHM2, SHM). METHODS: cRNA of human Na(+)/K(+)-ATPase α(2)- and β(1)-subunits were injected in Xenopus laevis oocytes. FHM2 or SHM mutations of residues located in putative α/β interacti...

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Bibliografische gegevens
Hoofdauteurs: Spiller, Susan, Friedrich, Thomas
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Baishideng Publishing Group Inc 2014
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4050117/
https://ncbi.nlm.nih.gov/pubmed/24921013
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4331/wjbc.v5.i2.240
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