Plectin-deficient myocyte cell models to study pathogenesis and phenotype rescue of plectinopathies
Winter, L; Wiche, G;
Plectin-deficient myocyte cell models to study pathogenesis and phenotype rescue of plectinopathies
Plectin is a ubiquitous multifunctional cytolinker protein expressed at high levels in muscle and skin. The most common disease caused by plectin deficiency, epidermolysis bullosa simplex (EBS)-MD, is characterized by muscular dystrophy and severe skin blistering. EBS-MD patients and plectin-deficient[for full text, please go to the a.m. URL]
57th Annual Meeting of the German Society for Neuropathology and Neuroanatomy (DGNN)
ddc: 610, 610 Medical sciences; Medicine
ddc: 610, 610 Medical sciences; Medicine
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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
Citations provided by BIP!popularityPopularity provided by BIP!
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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