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Dominant negative mutation in oxalate transporter SLC26A6 associated with enteric hyperoxaluria and nephrolithiasis

Document Type

Article

Author

Cornière, N.; Eladari, D.; Badreddine, A.; Dechaume, A.; Derhourhi, M.; Durand, E.; Vaillant, E.; Froguel, P.; Chambrey, R.; Bonnefond, A.; Thomson, R.B.; Karp, S.; Dynia, D.W.; Burlein, S.; Brinkmann, L.; Aronson, P.S.; Thauvin, S.; Villoutreix, B.O.

Source

In: Journal of Medical Genetics. (Journal of Medical Genetics, 2022, 59(11):1035-1043)

Subject

Language

English

ISSN

14686244
00222593

Online Access

Full Text (ProQuest Central) Full Text (BMJ Journals) Web of Science JCR 저널정보 Scopus Find it@PNU

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