Drosophila Carrying Pex3 or Pex16 Mutations Are Models of Zellweger Syndrome That Reflect Its Symptoms Associated with the Absence of Peroxisomes

The peroxisome biogenesis disorders (PBDs) are currently difficult-to-treat multiple-organ dysfunction disorders that result from the defective biogenesis of peroxisomes. Genes encoding Peroxins, which are required for peroxisome biogenesis or functions, are known causative genes of PBDs. The human...

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Detalles Bibliográficos
Autores principales: Nakayama, Minoru, Sato, Hiroyasu, Okuda, Takayuki, Fujisawa, Nao, Kono, Nozomu, Arai, Hiroyuki, Suzuki, Emiko, Umeda, Masato, Ishikawa, Hiroyuki O., Matsuno, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3149631/
https://www.ncbi.nlm.nih.gov/pubmed/21826223
http://dx.doi.org/10.1371/journal.pone.0022984

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