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Impaired neural development in a zebrafish model for Lowe syndrome

Lowe syndrome, which is characterized by defects in the central nervous system, eyes and kidneys, is caused by mutation of the phosphoinositide 5-phosphatase OCRL1. The mechanisms by which loss of OCRL1 leads to the phenotypic manifestations of Lowe syndrome are currently unclear, in part, owing to...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Ramirez, Irene Barinaga-Rementeria, Pietka, Grzegorz, Jones, David R., Divecha, Nullin, Alia, A., Baraban, Scott C., Hurlstone, Adam F. L., Lowe, Martin
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Oxford University Press 2012
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC3313792/
https://ncbi.nlm.nih.gov/pubmed/22210625
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr608
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