Joubert Syndrome, A Ciliopathy
Investigators at Neurogenetics Unit, Mendel Laboratory, Rome, and University of Salerno, Italy, review the clinical features and genetic basis of Joubert syndrome, overlap with other ciliopathies, and the multifaceted roles of primary cilia in CNS development.
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Materyal Türü: | Kitap |
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Pediatric Neurology Briefs Publishers,
2013-10-01T00:00:00Z.
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Online Erişim: | Connect to this object online. |
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Özet: | Investigators at Neurogenetics Unit, Mendel Laboratory, Rome, and University of Salerno, Italy, review the clinical features and genetic basis of Joubert syndrome, overlap with other ciliopathies, and the multifaceted roles of primary cilia in CNS development. |
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Diğer Bilgileri: | 1043-3155 2166-6482 10.15844/pedneurbriefs-27-10-8 |