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Proceedings of the National Academy of Sciences of the United States of America|January 11, 2000
Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa geneT Martinsson, A Oldfors, N Darin, et al.Journal of the American Academy of Child and Adolescent Psychiatry|May 1, 1991
Autism associated with marker chromosomeC Gillberg, S Steffenburg, J Wahlström, et al.Lakartidningen|February 1, 1995
[Gene amplification in viral CNS infections. Rapid diagnostic identification of herpesviruses]T Bergström, S Olofsson, M Studahl, et al.Neurology|March 13, 2002
Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with ageH Tajsharghi, L-E Thornell, N Darin, et al.Clinical Genetics|May 1, 1990
X-linked myotubular myopathy: a linkage studyC Darnfors, H E Larsson, A Oldfors, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1994
Dystonia and dyskinesia in glutaric aciduria type I: clinical heterogeneity and therapeutic considerationsM Kyllerman, O H Skjeldal, M Lundberg, et al.Clinical Genetics|February 1, 1994
The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9qJ Wahlström, L Ozelius, P Kramer, et al.Acta Paediatrica Scandinavica. Supplement|January 1, 1979
Effects on the child of alcohol abuse during pregnancy. Retrospective and prospective studiesR Olegård, K G Sabel, M Aronsson, et al.Neurology|August 1, 1992
Linkage studies in progressive myoclonus epilepsy: Unverricht-Lundborg and Lafora's diseasesA E Lehesjoki, M Koskiniemi, M Pandolfo, et al.Human Genetics|July 1, 1991
Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystoniaD Schuback, P Kramer, L Ozelius, et al.Pageof 9