Detalhe da pesquisa
1.
Mutations in WDR19 encoding the intraflagellar transport component IFT144 cause a broad spectrum of ciliopathies.
Pediatr Nephrol
; 29(8): 1451-6, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24504730
2.
Mutations in multiple PKD genes may explain early and severe polycystic kidney disease.
J Am Soc Nephrol
; 22(11): 2047-56, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22034641
3.
Phenotypic Spectrum of Children with Nephronophthisis and Related Ciliopathies.
Clin J Am Soc Nephrol
; 12(12): 1974-1983, 2017 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29146700