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Crystallographic characterization of CCG repeats

CCG repeats are highly over-represented in exons of the human genome. Usually they are located in the 5′ UTR but are also abundant in translated sequences. The CCG repeats are associated with three tri-nucleotide repeat disorders: Huntington’s disease, myotonic dystrophy type 1 and chromosome X-link...

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Autors principals: Kiliszek, Agnieszka, Kierzek, Ryszard, Krzyzosiak, Wlodzimierz J., Rypniewski, Wojciech
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2012
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3439926/
https://ncbi.nlm.nih.gov/pubmed/22718980
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gks557
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