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Brain and Eye Malformations Resembling Walker–Warburg Syndrome Are Recapitulated in Mice by Dystroglycan Deletion in the Epiblast

Walker–Warburg syndrome (WWS) is a severe congenital disease that is characterized by brain and eye malformations and lethality during the first year of life. Genetic mutations have been identified in a subset of WWS patients, but a majority of clinical cases have unknown etiologies. POMT1 and POMT2...

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Detalhes bibliográficos
Main Authors: Satz, Jakob S., Barresi, Rita, Durbeej, Madeleine, Willer, Tobias, Turner, Amy, Moore, Steven A., Campbell, Kevin P.
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2008
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2714190/
https://ncbi.nlm.nih.gov/pubmed/18923033
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.2457-08.2008
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