Autor: |
Brittney, Knott, Matthew A, Kocher, Henry A, Paz, Shelby E, Hamm, William, Fink, Jordan, Mason, Robert W, Grange, Umesh D, Wankhade, Deborah J, Good |
Rok vydání: |
2021 |
Předmět: |
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Zdroj: |
Nutrients. 14(4) |
ISSN: |
2072-6643 |
Popis: |
Prader-Willi Syndrome (PWS) is a human genetic condition that affects up to 1 in 10,000 live births. Affected infants present with hypotonia and developmental delay. Hyperphagia and increasing body weight follow unless drastic calorie restriction is initiated. Recently, our laboratory showed that one of the genes in the deleted locus causative for PWS |
Databáze: |
OpenAIRE |
Externí odkaz: |
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