TY  - JOUR 
AU  - Toustrup-Jensen, MS
AU  - Einholm, AP
AU  - Schack, VR
AU  - Nielsen, HN
AU  - Holm, R
AU  - Sobrido Gómez, María Jesús
AU  - Andersen, JP
AU  - Clausen, T
AU  - Vilsen, B
PY  - 2014
SN  - 0021-9258
UR  - http://hdl.handle.net/20.500.11940/6257
AB  - The neurological disorders familial hemiplegic migraine type 2 (FHM2), alternating hemiplegia of childhood (AHC), and rapid-onset dystonia parkinsonism (RDP) are caused by mutations of Na(+),K(+)-ATPase α2 and α3 isoforms, expressed in glial and...
LA  - eng
KW  - Animals
KW  - COS Cells
KW  - Chlorocebus aethiops
KW  - Dystonic Disorders
KW  - Humans
KW  - Ion Transport
KW  - Migraine with Aura
KW  - Mutation, Missense
KW  - Potassium
KW  - Protein Structure, Tertiary
KW  - Rats
KW  - Sodium
KW  - Sodium-Potassium-Exchanging ATPase
KW  - Enzyme Mutation
KW  - Familial Hemiplegic Migraine
KW  - Intracellular Sodium
KW  - Membrane Transport
KW  - Na,K-ATPase
KW  - Neurological Diseases
KW  - Rapid-onset Dystonia Parkinsonism
KW  - Sodium Transport
TI  - Relationship between Intracellular Na+ Concentration and Reduced Na+ Affinity in Na+,K+-ATPase Mutants Causing Neurological Disease
DO  - 10.1074/jbc.M113.543272
T2  - JOURNAL OF BIOLOGICAL CHEMISTRY
M2  - 3186
VL  - 289
ER  -