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Brain involvement in muscular dystrophies with defective dystroglycan glycosylation

Brain involvement in muscular dystrophies with defective dystroglycan glycosylation

Dettagli Bibliografici
Autori principali: Clement, E, Mercuri, E, Godfrey, C, Smith, J, Robb, S, Kinali, M, Straub, V, Bushby, K, Manzur, A, Talim, B, Cowan, F, Quinlivan, R, Klein, A, Longman, C, McWilliam, R, Topaloglu, H, Mein, R, Abbs, S, North, K, Barkovich, A, Rutherford, M, Muntoni, F
Natura: Journal article
Pubblicazione: 2008
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Documenti analoghi

  • Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan
    di: Godfrey, C, et al.
    Pubblicazione: (2007)
  • A Comparative Study of α-Dystroglycan Glycosylation in Dystroglycanopathies Suggests that the Hypoglycosylation of α-Dystroglycan Does Not Consistently Correlate with Clinical Severity
    di: Jimenez-Mallebrera, C, et al.
    Pubblicazione: (2009)
  • Relative frequency of congenital muscular dystrophy subtypes: Analysis of the UK diagnostic service 2001–2008
    di: Clement, E, et al.
    Pubblicazione: (2012)
  • Flow cytometry for the analysis of α-dystroglycan glycosylation in fibroblasts from patients with dystroglycanopathies.
    di: Elizabeth Stevens, et al.
    Pubblicazione: (2013-01-01)
  • Functional glycosylation of dystroglycan is crucial for thymocyte development in the mouse.
    di: Li-Ying Liou, et al.
    Pubblicazione: (2010-03-01)

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