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A Melberg

Showing results (21-30 of 25) with videos related to

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European Journal of Human Genetics : EJHG|April 10, 1999
Analysis of the trinucleotide CAG repeat from the human mitochondrial DNA polymerase gene in healthy and diseased individualsA Rovio, V Tiranti, A L Bednarz, et al.
Annals of Neurology|September 2, 2000
Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy linked to chromosome 10qA Melberg, A Oldfors, C Blomström-Lundqvist, et al.
Human Molecular Genetics|March 4, 2000
Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patientsG V Börner, M Zeviani, V Tiranti, et al.
Neurology|January 5, 2002
CSF hypocretin/orexin levels in narcolepsy and other neurological conditionsB Ripley, S Overeem, N Fujiki, et al.
Neurology|September 29, 2004
Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutationE E Kors, A Melberg, K R J Vanmolkot, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

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Pageof 3
You have reached the last page of results.This site can display upto 25 results.
European Journal of Human Genetics : EJHG|April 10, 1999
Analysis of the trinucleotide CAG repeat from the human mitochondrial DNA polymerase gene in healthy and diseased individualsA Rovio, V Tiranti, A L Bednarz, et al.
Annals of Neurology|September 2, 2000
Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy linked to chromosome 10qA Melberg, A Oldfors, C Blomström-Lundqvist, et al.
Human Molecular Genetics|March 4, 2000
Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patientsG V Börner, M Zeviani, V Tiranti, et al.
Neurology|January 5, 2002
CSF hypocretin/orexin levels in narcolepsy and other neurological conditionsB Ripley, S Overeem, N Fujiki, et al.
Neurology|September 29, 2004
Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutationE E Kors, A Melberg, K R J Vanmolkot, et al.
Pageof 3