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Cilia in the nervous system: linking cilia function and neurodevelopmental disorders
PURPOSE OF REVIEW: Ciliopathies are genetic disorders caused by defects of primary ciliary structure and/or function and are characterized by pleiotropic clinical features. The ciliopathies include several partially overlapping syndromes such as Joubert syndrome, Bardet–Biedl syndrome and Meckel–Gru...
Bewaard in:
| Hoofdauteurs: | , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2011
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3984876/ https://ncbi.nlm.nih.gov/pubmed/21386674 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/WCO.0b013e3283444d05 |
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