Dysferlin Deficiency Shows Compensatory Induction of Rab27A/Slp2a That May Contribute to Inflammatory Onset

Mutations in the dysferlin gene cause limb girdle muscular dystrophy 2B (LGMD2B) and Miyoshi myopathy. Dysferlin-deficient cells show abnormalities in vesicular traffic and membrane repair although onset of symptoms is not commonly seen until the late teenage years and is often associated with subac...

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Bibliografische gegevens
Hoofdauteurs: Kesari, Akanchha, Fukuda, Mitsunori, Knoblach, Susan, Bashir, Rumaisa, Nader, Gustavo A., Rao, Deepak, Nagaraju, Kanneboyina, Hoffman, Eric P.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Society for Investigative Pathology 2008
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2570137/
https://ncbi.nlm.nih.gov/pubmed/18832576
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/ajpath.2008.080098
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