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Impaired IGF1-GH axis and new therapeutic options in Alström Syndrome patients: a case series
BACKGROUND: Defects of the primary cilium and its anchoring structure, the basal body, cause a number of human genetic disorders, collectively termed ciliopathies: primary ciliary dyskinesia, Bardet-Biedl syndrome, polycystic kidney and liver disease, nephronophthisis, Alström syndrome, Meckel-Grube...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2648950/ https://ncbi.nlm.nih.gov/pubmed/19128470 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1757-1626-2-19 |
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