Primary Hyperoxaluria Type III Gene HOGA1 (Formerly DHDPSL) as a Possible Risk Factor for Idiopathic Calcium Oxalate Urolithiasis

SUMMARY: BACKGROUND AND OBJECTIVES: Primary hyperoxaluria types I and II (PHI and PHII) are rare monogenic causes of hyperoxaluria and calcium oxalate urolithiasis. Recently, we described type III, due to mutations in HOGA1 (formerly DHDPSL), hypothesized to cause a gain of mitochondrial 4-hydroxy-2...

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Detalhes bibliográficos
Main Authors: Monico, Carla G., Rossetti, Sandro, Belostotsky, Ruth, Cogal, Andrea G., Herges, Regina M., Seide, Barbara M., Olson, Julie B., Bergstrahl, Eric J., Williams, Hugh J., Haley, William E., Frishberg, Yaacov, Milliner, Dawn S.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2011
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3358997/
https://ncbi.nlm.nih.gov/pubmed/21896830
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.02760311
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