Single point mutation in Rabenosyn-5 in a female with intractable seizures and evidence of defective endocytotic trafficking

BACKGROUND: We report a 6.5 year-old female with a homozygous missense mutation in ZFYVE20, encoding Rabenosyn-5 (Rbsn-5), a highly conserved multi-domain protein implicated in receptor-mediated endocytosis. The clinical presentation includes intractable seizures, developmental delay, microcephaly,...

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Detalles Bibliográficos
Autores principales: Stockler, Sylvia, Corvera, Silvia, Lambright, David, Fogarty, Kevin, Nosova, Ekaterina, Leonard, Deborah, Steinfeld, Robert, Ackerley, Cameron, Shyr, Casper, Au, Nicolas, Selby, Kathrin, van Allen, Margot, Vallance, Hilary, Wevers, Ron, Watkins, David, Rosenblatt, David, Ross, Colin J, Conibear, Elizabeth, Wasserman, Wyeth, van Karnebeek, Clara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177245/
https://www.ncbi.nlm.nih.gov/pubmed/25233840
http://dx.doi.org/10.1186/s13023-014-0141-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177245/
https://www.ncbi.nlm.nih.gov/pubmed/25233840
http://dx.doi.org/10.1186/s13023-014-0141-5

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