Detalhe da pesquisa
1.
Consanguinity and prevalence patterns of inherited disease in the UK Pakistani community.
Hum Hered
; 77(1-4): 207-16, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25060285
2.
Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus.
Nat Genet
; 38(8): 917-20, 2006 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-16845398
3.
Risk factors for congenital anomaly in a multiethnic birth cohort: an analysis of the Born in Bradford study.
Lancet
; 382(9901): 1350-9, 2013 Oct 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-23830354
4.
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response.
Nat Genet
; 41(7): 829-32, 2009 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19525956
5.
Clinical and molecular phenotype of Aicardi-Goutieres syndrome.
Am J Hum Genet
; 81(4): 713-25, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17846997