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Different atrophy-hypertrophy transcription pathways in muscles affected by severe and mild spinal muscular atrophy

BACKGROUND: Spinal muscular atrophy (SMA) is a neurodegenerative disorder associated with mutations of the survival motor neuron gene SMN and is characterized by muscle weakness and atrophy caused by degeneration of spinal motor neurons. SMN has a role in neurons but its deficiency may have a direct...

詳細記述

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書誌詳細
主要な著者: Millino, Caterina, Fanin, Marina, Vettori, Andrea, Laveder, Paolo, Mostacciuolo, Maria Luisa, Angelini, Corrado, Lanfranchi, Gerolamo
フォーマット: Artigo
言語:Inglês
出版事項: BioMed Central 2009
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2676312/
https://ncbi.nlm.nih.gov/pubmed/19351384
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1741-7015-7-14
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