Contributions of Rare Gene Variants to Familial and Sporadic FSGS

BACKGROUND: Over the past two decades, the importance of genetic factors in the development of FSGS has become increasingly clear. However, despite many known monogenic causes of FSGS, single gene defects explain only 30% of cases. METHODS: To investigate mutations underlying FSGS, we sequenced 662...

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Detalhes bibliográficos
Publicado no:J Am Soc Nephrol
Main Authors: Wang, Minxian, Chun, Justin, Genovese, Giulio, Knob, Andrea U., Benjamin, Ava, Wilkins, Maris S., Friedman, David J., Appel, Gerald B., Lifton, Richard P., Mane, Shrikant, Pollak, Martin R.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2019
Assuntos:
Basic Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6727251/
https://ncbi.nlm.nih.gov/pubmed/31308072
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2019020152
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