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1. Die myopathische Form des Koenzym Q10-Mangels


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2. Biobanking in rare disorders.

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http://hdl.handle.net/10822/515155
http://xr8el9yb8v.search.serialssolutions.com/?version=1.0&url_ver=Z39.88-2004&rft_val_fmt=info:o...  

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3. miR-411 is up-regulated in FSHD myoblasts and suppresses myogenic factors

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4. miR-411 is up-regulated in FSHD myoblasts and suppresses myogenic factors

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3637251
http://www.ncbi.nlm.nih.gov/pubmed/23561550  
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5. Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A - evidence for “double trouble” overlapping syndromes

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848428
http://www.ncbi.nlm.nih.gov/pubmed/24041033  
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6. miR-411 is up-regulated in FSHD myoblasts and suppresses myogenic factors


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7. Immortalized myogenic cells from congenital muscular dystrophy type1A patients recapitulate aberrant caspase activation in pathogenesis: a new tool for MDC1A research

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8. Flow Cytometry for the Analysis of α-Dystroglycan Glycosylation in Fibroblasts from Patients with Dystroglycanopathies

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718821
http://www.ncbi.nlm.nih.gov/pubmed/23894383  
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9. Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery–Dreifuss muscular dystrophy

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC
http://www.ncbi.nlm.nih.gov/pubmed/25454731  
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10. Immortalized myogenic cells from congenital muscular dystrophy type1A patients recapitulate aberrant caspase activation in pathogenesis: a new tool for MDC1A research

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906772
http://www.ncbi.nlm.nih.gov/pubmed/24314268  
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