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Adrian J Waite

Showing results (11-20 of 16) with videos related to

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Scientific Reports|July 26, 2017
Ryanodine receptors are part of the myospryn complex in cardiac muscleMatthew A Benson, Caroline L Tinsley, Adrian J Waite, et al.
Frontiers in Molecular Biosciences|January 1, 2024
Misfolding of fukutin-related protein (FKRP) variants in congenital and limb girdle muscular dystrophiesChristopher T Esapa, R A Jeffrey McIlhinney, Adrian J Waite, et al.
Annals of Neurology|June 6, 2015
C9orf72 ablation in mice does not cause motor neuron degeneration or motor deficitsMax Koppers, Anna M Blokhuis, Henk-Jan Westeneng, et al.
Acta Neuropathologica|July 3, 2013
Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementiaPietro Fratta, Mark Poulter, Tammaryn Lashley, et al.
Journal of Neurology|September 12, 2014
SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotypeKathryn J Peall, Manju A Kurian, Mark Wardle, et al.
Brain : a Journal of Neurology|February 1, 2013
SGCE mutations cause psychiatric disorders: clinical and genetic characterizationKathryn J Peall, Daniel J Smith, Manju A Kurian, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Scientific Reports|July 26, 2017
Ryanodine receptors are part of the myospryn complex in cardiac muscleMatthew A Benson, Caroline L Tinsley, Adrian J Waite, et al.
Frontiers in Molecular Biosciences|January 1, 2024
Misfolding of fukutin-related protein (FKRP) variants in congenital and limb girdle muscular dystrophiesChristopher T Esapa, R A Jeffrey McIlhinney, Adrian J Waite, et al.
Annals of Neurology|June 6, 2015
C9orf72 ablation in mice does not cause motor neuron degeneration or motor deficitsMax Koppers, Anna M Blokhuis, Henk-Jan Westeneng, et al.
Acta Neuropathologica|July 3, 2013
Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementiaPietro Fratta, Mark Poulter, Tammaryn Lashley, et al.
Journal of Neurology|September 12, 2014
SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotypeKathryn J Peall, Manju A Kurian, Mark Wardle, et al.
Brain : a Journal of Neurology|February 1, 2013
SGCE mutations cause psychiatric disorders: clinical and genetic characterizationKathryn J Peall, Daniel J Smith, Manju A Kurian, et al.
Pageof 2