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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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Bibliografiske detaljer
Main Authors: Deltas, Constantinos, Pierides, Alkis, Voskarides, Konstantinos
Format: Artigo
Sprog:Inglês
Udgivet: Springer-Verlag 2011
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3382641/
https://ncbi.nlm.nih.gov/pubmed/21688191
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-011-1935-5
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