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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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| Auteurs principaux: | , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BMJ Group
2006
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| Sujets: | |
| Accès en ligne: | 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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