Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man

Detalles Bibliográficos
Autores principales: Tuschl, Karin, Clayton, Peter T., Gospe, Sidney M., Gulab, Shamshad, Ibrahim, Shahnaz, Singhi, Pratibha, Aulakh, Roosy, Ribeiro, Reinaldo T., Barsottini, Orlando G., Zaki, Maha S., Del Rosario, Maria Luz, Dyack, Sarah, Price, Victoria, Rideout, Andrea, Gordon, Kevin, Wevers, Ron A., Chong, W.K. ‘‘Kling’’, Mills, Philippa B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Correction
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974105/
https://www.ncbi.nlm.nih.gov/pubmed/27486784
http://dx.doi.org/10.1016/j.ajhg.2016.07.015

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974105/
https://www.ncbi.nlm.nih.gov/pubmed/27486784
http://dx.doi.org/10.1016/j.ajhg.2016.07.015

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