Lack of Mid1, the Mouse Ortholog of the Opitz Syndrome Gene, Causes Abnormal Development of the Anterior Cerebellar Vermis

Opitz G/BBB syndrome (OS) is a genetic disorder characterized by midline developmental defects. Male patients with the X-linked form of OS, caused by loss-of-function mutations in the MID1 gene, show high variability of the clinical signs. MID1 encodes a ubiquitin ligase that controls phosphatase 2A...

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Vydáno v:J Neurosci
Hlavní autoři: Lancioni, Alessio, Pizzo, Mariateresa, Fontanella, Bianca, Ferrentino, Rosa, Napolitano, Luisa M. R., De Leonibus, Elvira, Meroni, Germana
Médium: Artigo
Jazyk:Inglês
Vydáno: Society for Neuroscience 2010
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6633954/
https://ncbi.nlm.nih.gov/pubmed/20181585
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.4196-09.2010
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