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Autor:
Kaivola, K. (Karri), Kiviharju, A. (Anna), Jansson, L. (Lilja), Rantalainen, V. (Ville), Eriksson, J. G. (Johan G.), Strandberg, T. E. (Timo E.), Laaksovirta, H. (Hannu), Renton, A. E. (Alan E.), Traynor, B. J. (Bryan J.), Myllykangas, L. (Liisa), Tienari, P. J. (Pentti J.)
The hexanucleotide repeat expansion in C9orf72 is a common cause of amyotrophic lateral sclerosis/frontotemporal dementia and also rarely found in other psychiatric and neurodegenerative conditions. Alleles with >30 repeats are often considered an ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2423::4d3821d955d7f2ef55bf7183f660d224
http://urn.fi/urn:nbn:fi-fe202002104962
http://urn.fi/urn:nbn:fi-fe202002104962