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Reproductive dysfunction and decreased GnRH neurogenesis in a mouse model of CHARGE syndrome
CHARGE is a multiple congenital anomaly disorder and a common cause of pubertal defects, olfactory dysfunction, growth delays, deaf-blindness, balance disorders and congenital heart malformations. Mutations in CHD7, the gene encoding chromodomain helicase DNA binding protein 7, are present in 60–80%...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2011
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3140819/ https://ncbi.nlm.nih.gov/pubmed/21596839 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr216 |
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