A protocol for the identification and validation of novel genetic causes of kidney disease

BACKGROUND: Genetic renal diseases (GRD) are a heterogeneous and incompletely understood group of disorders accounting for approximately 10 % of those diagnosed with kidney disease. The advent of Next Generation sequencing and new approaches to disease modelling may allow the identification and vali...

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Detalles Bibliográficos
Autores principales: Mallett, Andrew, Patel, Chirag, Maier, Barbara, McGaughran, Julie, Gabbett, Michael, Takasato, Minoru, Cameron, Anne, Trnka, Peter, I. Alexander, Stephen, Rangan, Gopala, Tchan, Michel C., Caruana, Georgina, John, George, Quinlan, Cathy, McCarthy, Hugh J., Hyland, Valentine, E. Hoy, Wendy, Wolvetang, Ernst, Taft, Ryan, Simons, Cas, Healy, Helen, Little, Melissa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Study Protocol
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4570515/
https://www.ncbi.nlm.nih.gov/pubmed/26374634
http://dx.doi.org/10.1186/s12882-015-0148-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4570515/
https://www.ncbi.nlm.nih.gov/pubmed/26374634
http://dx.doi.org/10.1186/s12882-015-0148-8

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