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High Plasma Neurotensin Levels in Children with Prader–Willi Syndrome
Prader-Willi syndrome (PWS) is an obesity-related genetic condition, most commonly due to a paternal deletion of the chromosome 15q11-q13 region. PWS is characterized by growth hormone deficiency, infantile hypotonia and feeding problems, hypogenitalism/hypogonadism, increased pain threshold and the...
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| Publicado en: | Am J Med Genet A |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2015
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6686671/ https://ncbi.nlm.nih.gov/pubmed/25847417 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.37103 |
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