Loss-of-function mutations of SCN10A encoding Na(V)1.8 α subunit of voltage-gated sodium channel in patients with human kidney stone disease

Human kidney stone disease (KSD) causes significant morbidity and public health burden worldwide. The etiology of KSD is heterogeneous, ranging from monogenic defects to complex interaction between genetic and environmental factors. However, the genetic defects causing KSD in the majority of affecte...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Pubblicato in:Sci Rep
Autori principali: Nettuwakul, Choochai, Praditsap, Oranud, Sawasdee, Nunghathai, Rungroj, Nanyawan, Ruamyod, Katesirin, Watanapa, Wattana B., Junking, Mutita, Sangnual, Sittideth, Sritippayawan, Suchai, Cheunsuchon, Boonyarit, Chuawattana, Duangporn, Rojsatapong, Santi, Chaowagul, Wipada, Dib-Hajj, Sulayman D., Waxman, Stephen G., Yenchitsomanus, Pa-thai
Natura: Artigo
Lingua:Inglês
Pubblicazione: Nature Publishing Group UK 2018
Soggetti:
Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6041274/
https://ncbi.nlm.nih.gov/pubmed/29992996
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-018-28623-3
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi