The role of molecular genetics in diagnosing familial hematuria(s)

Familial microscopic hematuria (MH) of glomerular origin represents a heterogeneous group of monogenic conditions involving several genes, some of which remain unknown. Recent advances have increased our understanding and our ability to use molecular genetics for diagnosing such patients, enabling u...

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Detalles Bibliográficos
Autores principales: Deltas, Constantinos, Pierides, Alkis, Voskarides, Konstantinos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382641/
https://www.ncbi.nlm.nih.gov/pubmed/21688191
http://dx.doi.org/10.1007/s00467-011-1935-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382641/
https://www.ncbi.nlm.nih.gov/pubmed/21688191
http://dx.doi.org/10.1007/s00467-011-1935-5

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