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The cystic fibrosis transmembrane conductance regulator (Cftr) modulates the timing of puberty in mice
BACKGROUND: Delayed puberty is common among individuals with cystic fibrosis (CF) and is usually attributed to chronic disease and/or poor nutrition. However, it has recently been recognised that pubertal delay can occur even in the setting of good nutritional and clinical status. This finding, alon...
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| Главные авторы: | , , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BMJ Group
2006
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2564546/ https://ncbi.nlm.nih.gov/pubmed/16740913 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2005.032839 |
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