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Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers

Facioscapulohumeral muscular dystrophy (FSHD) is a progressive muscle disorder that has been associated with a contraction of 3.3-kb repeats on chromosome 4q35. FSHD is characterized by a wide clinical inter- and intrafamilial variability, ranging from wheelchair-bound patients to asymptomatic carri...

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Detalhes bibliográficos
Main Authors: Arashiro, Patricia, Eisenberg, Iris, Kho, Alvin T., Cerqueira, Antonia M. P., Canovas, Marta, Silva, Helga C. A., Pavanello, Rita C. M., Verjovski-Almeida, Sergio, Kunkel, Louis M., Zatz, Mayana
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2009
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2664154/
https://ncbi.nlm.nih.gov/pubmed/19339494
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0901573106
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