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Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6.
Eur J Hum Genet. 2014 Feb;22(2):208-15. doi: 10.1038/ejhg.2013.108. Epub 2013 May 29.
Eur J Hum Genet. 2014.
PMID: 23714752
Free PMC article.
DNA damage, somatic aneuploidy, and malignant sarcoma susceptibility in muscular dystrophies.
Schmidt WM, Uddin MH, Dysek S, Moser-Thier K, Pirker C, Höger H, Ambros IM, Ambros PF, Berger W, Bittner RE.
Schmidt WM, et al. Among authors: dysek s.
PLoS Genet. 2011 Apr;7(4):e1002042. doi: 10.1371/journal.pgen.1002042. Epub 2011 Apr 14.
PLoS Genet. 2011.
PMID: 21533183
Free PMC article.
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Voltage-gated ion channel dysfunction precedes cardiomyopathy development in the dystrophic heart.
Koenig X, Dysek S, Kimbacher S, Mike AK, Cervenka R, Lukacs P, Nagl K, Dang XB, Todt H, Bittner RE, Hilber K.
Koenig X, et al. Among authors: dysek s.
PLoS One. 2011;6(5):e20300. doi: 10.1371/journal.pone.0020300. Epub 2011 May 23.
PLoS One. 2011.
PMID: 21677768
Free PMC article.
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