Caricamento...
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...
Salvato in:
| Autori principali: | , , , |
|---|---|
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BMJ Group
2006
|
| Soggetti: | |
| Accesso online: | 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 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|