RET gene mutations are not a common cause of congenital solitary functioning kidney in adults

Detalles Bibliográficos
Autores principales: Oram, Richard A., Edghill, Emma L., Woolf, Adrian S., Hennekam, R. C., Ellard, Sian, Hattersley, A. T., Bingham, Coralie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Letters
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421350/
https://www.ncbi.nlm.nih.gov/pubmed/25949327
http://dx.doi.org/10.1093/ndtplus/sfn204

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421350/
https://www.ncbi.nlm.nih.gov/pubmed/25949327
http://dx.doi.org/10.1093/ndtplus/sfn204

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