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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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Bibliografische gegevens
Gepubliceerd in:Am J Med Genet A
Hoofdauteurs: Butler, Merlin G., Hossain, Waheeda A., Tessman, Robert, Krishnamurthy, Partha K.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2018
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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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