X-linked microtubule-associated protein, Mid1, regulates axon development
X-linked microtubule-associated protein, Mid1, regulates axon development
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Publisher
Washington, DC: National Academy of Sciences
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Language
English
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Publisher
Washington, DC: National Academy of Sciences
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Scope and Contents
Contents
Opitz syndrome (OS) is a genetic neurological disorder. The gene responsible for the X-linked form of OS, Midline-1 (MID1), encodes an E3 ubiquitin ligase that regulates the degradation of the catalytic subunit of protein phosphatase 2A (PP2Ac). However, how Mid1 functions during neural development is largely unknown. In this study, we provide data...
Alternative Titles
Full title
X-linked microtubule-associated protein, Mid1, regulates axon development
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Record Identifier
TN_cdi_pubmed_primary_24194544
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmed_primary_24194544
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ISSN
0027-8424
E-ISSN
1091-6490
DOI
10.1073/pnas.1303687110
