Carregant...
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...
Guardat en:
| Autors principals: | , , , |
|---|---|
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMJ Group
2006
|
| Matèries: | |
| Accés en línia: | 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 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|