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Anders Oldfors - University of Gothenburg, Sweden Till startsida
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Anders Oldfors


Anders Oldfors
+46 31-342 2084

Postal Address: Box 100, 40530 Göteborg
Visiting Address: Gula stråket 8 , 41345 Göteborg

Department of Laboratory Medicine at Institute of Biomedicine (More Information)
Sahlgrenska universitetssjukhuset
413 45 Göteborg
Visiting Address: Gula stråket 8 , 413 45 Göteborg

Latest publications

Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24
Carola Oldfors Hedberg, Alexandra Abramsson, D. P. S. Osborn, O. Danielsson, A. Fazlinezhad et al.
Hum Mol Genet, Journal article 2019
Journal article

Loss of Sarcomeric Scaffolding as a Common Baseline Histopathologic Lesion in Titin-Related Myopathies
R. Ávila-Polo, E. Malfatti, X. Lornage, C. Cheraud, I. Nelson et al.
Journal of Neuropathology and Experimental Neurology, Journal article 2018
Journal article

Showing 81 - 90 of 140


Human disease caused by loss of fast IIa myosin heavy chain due to recessive MYH2 mutations.
Homa Tajsharghi, David Hilton-Jones, Olayinka Raheem, Anna Maija Saukkonen, Anders Oldfors et al.
Brain : a journal of neurology, Journal article 2010
Journal article


A novel homozygous RRM2B missense mutation in association with severe mtDNA depletion.
Gittan Kollberg, Niklas Darin, Karin Benan, Ali-Reza Moslemi, Sigurd Lindal et al.
Neuromuscular disorders : NMD, Journal article 2009
Journal article

Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy.
Rita Horvath, John P Kemp, Helen A L Tuppen, Gavin Hudson, Anders Oldfors et al.
Brain : a journal of neurology, Journal article 2009
Journal article

A patient with two mitochondrial DNA mutations causing PEO and LHON.
Atle Melberg, Ali-Reza Moslemi, Oscar Palm, Raili Raininko, Erik Stålberg et al.
European journal of medical genetics, Journal article 2009
Journal article

"Necklace" fibers, a new histological marker of late-onset MTM1-related centronuclear myopathy.
Jorge A Bevilacqua, Marc Bitoun, Valérie Biancalana, Anders Oldfors, Gisela Stoltenburg et al.
Acta neuropathologica, Journal article 2009
Journal article


New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutations.
Monica Ohlsson, S Quijano-Roy, Niklas Darin, G Brochier, E Lacène et al.
Neurology, Journal article 2008
Journal article

Showing 81 - 90 of 140

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Utskriftsdatum: 2019-09-15