Mutations in the Na+/K+-ATPase α3 Gene ATP1A3 Are Associated with Rapid-Onset Dystonia Parkinsonism
Top Cited Papers
- 1 July 2004
- Vol. 43 (2) , 169-175
- https://doi.org/10.1016/j.neuron.2004.06.028
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Novel mutations in the Na+, K+‐ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsionsAnnals of Neurology, 2003
- ATP-induced conformational changes of the nucleotide-binding domain of Na,K-ATPaseNature Structural & Molecular Biology, 2003
- The Na,K-ATPase α2 Isoform Is Expressed in Neurons, and Its Absence Disrupts Neuronal Activity in Newborn MiceJournal of Biological Chemistry, 2003
- Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump α2 subunit associated with familial hemiplegic migraine type 2Nature Genetics, 2003
- Possible sporadic rapid‐onset dystonia–parkinsonismMovement Disorders, 2002
- Structural similarities of Na,K-ATPase and SERCA, the Ca2+-ATPase of the sarcoplasmic reticulumBiochemical Journal, 2001
- Structure of the 5th transmembrane segment of the Na,K-ATPase α subunit: a cysteine-scanning mutagenesis studyFEBS Letters, 2000
- Comparative Protein Structure Modeling of Genes and GenomesAnnual Review of Biophysics, 2000
- Scanning Mutagenesis Reveals a Similar Pattern of Mutation Sensitivity in Transmembrane Sequences M4, M5, and M6, but Not in M8, of the Ca2+-ATPase of Sarcoplasmic Reticulum (SERCA1a)Published by Elsevier ,1996
- Short and Long Range Functions of Amino Acids in the Transmembrane Region of the Sarcoplasmic Reticulum ATPasePublished by Elsevier ,1996