Загрузка...
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...
Сохранить в:
| Опубликовано в: : | Am J Med Genet A |
|---|---|
| Главные авторы: | , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2015
|
| Предметы: | |
| Online-ссылка: | 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 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|