Messenger RNA processing is altered in autosomal dominant leukodystrophy(†)

Adult-onset autosomal dominant leukodystrophy (ADLD) is a slowly progressive neurological disorder characterized by autonomic dysfunction, followed by cerebellar and pyramidal features. ADLD is caused by duplication of the lamin B1 gene (LMNB1), which leads to its increased expression. The molecular...

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Bibliografske podrobnosti
izdano v:Hum Mol Genet
Main Authors: Bartoletti-Stella, Anna, Gasparini, Laura, Giacomini, Caterina, Corrado, Patrizia, Terlizzi, Rossana, Giorgio, Elisa, Magini, Pamela, Seri, Marco, Baruzzi, Agostino, Parchi, Piero, Brusco, Alfredo, Cortelli, Pietro, Capellari, Sabina
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2015
Teme:
Articles
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4406291/
https://ncbi.nlm.nih.gov/pubmed/25637521
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv034
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