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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:J Am Soc Nephrol
Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: American Society of Nephrology 2019
Matèries:
Basic Research
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars