Mutant (CCTG)n Expansion Causes Abnormal Expression of Zinc Finger Protein 9 (ZNF9) in Myotonic Dystrophy Type 2

The mutation that underlies myotonic dystrophy type 2 (DM2) is a (CCTG)n expansion in intron 1 of zinc finger protein 9 (ZNF9). It has been suggested that ZNF9 is of no consequence for disease pathogenesis. We determined the expression levels of ZNF9 during muscle cell differentiation and in DM2 mus...

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Main Authors: Raheem, Olayinka, Olufemi, Shodimu-Emmanuel, Bachinski, Linda L., Vihola, Anna, Sirito, Mario, Holmlund-Hampf, Jeanette, Haapasalo, Hannu, Li, Yi-Ping, Udd, Bjarne, Krahe, Ralf
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2010
Assuntos:
Regular Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2993290/
https://ncbi.nlm.nih.gov/pubmed/20971734
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/ajpath.2010.100179
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