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Preliminary Observations of Mitochondrial Dysfunction in Prader-Willi Syndrome
Prader-Willi syndrome (PWS) is a complex multi-system disorder due to errors in genomic imprinting with severe hypotonia, decreased muscle mass, poor suckling, feeding problems and failure to thrive during infancy, growth and other hormone deficiency, childhood-onset hyperphagia and subsequent obesi...
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| Gepubliceerd in: | Am J Med Genet A |
|---|---|
| Hoofdauteurs: | , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2018
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6312481/ https://ncbi.nlm.nih.gov/pubmed/30289596 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.40526 |
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