Detalhe da pesquisa
1.
A whole genome SNP genotyping by DNA microarray and candidate gene association study for kidney stone disease.
BMC Med Genet
; 15: 50, 2014 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-24886237
2.
Evidence suggesting a genetic contribution to kidney stone in northeastern Thai population.
Urol Res
; 37(3): 141-6, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19387627
3.
Loss-of-function mutations of SCN10A encoding NaV1.8 α subunit of voltage-gated sodium channel in patients with human kidney stone disease.
Sci Rep
; 8(1): 10453, 2018 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29992996
4.
Association between human prothrombin variant (T165M) and kidney stone disease.
PLoS One
; 7(9): e45533, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23029076
5.
Prothrombin haplotype associated with kidney stone disease in Northeastern Thai patients.
Urology
; 77(1): 249.e17-23, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21067798