Neurology · 2004 · 90 citations · 8 references
MedicineMolecular GeneticsPathologyCellular PathologyGeneral PathologyMolecular PathologyConnective Tissue DiseasesConnective Tissue DisordersGenetic Disease PathologyGenetic DisordersMuscle PathologyMyofibrillar Myopathy
The authors identified eight patients with Ullrich disease in whom collagen VI was present in the interstitium but was absent from the sarcolemma. By electron microscopy, collagen VI in the interstitium was never linked to the basal lamina. These findings suggest that in these patients it is not the total absence of collagen VI from the muscle but the failure of collagen VI to anchor the basal lamina to the interstitium that is the cause of Ullrich disease. Only one of the patients had a mutation in the collagen VI gene, suggesting that the primary abnormality in most of the patients involved some other molecules.
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Mutations in the integrin α7 gene cause congenital myopathy
Yukiko Hayashi, Fan-Li Chou, Eva Engvall et al. · Nature Genetics · 1998 · 358 citations
Collagen VI involvement in Ullrich syndrome
Eugenio Mercuri, Yeliz Yuva, S. Brown et al. · Neurology · 2002 · 102 citations