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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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| 出版年: | Am J Med Genet A |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2018
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| 主題: | |
| オンライン･アクセス: | 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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