Detalhe da pesquisa
1.
Clinical features and possible founder mutation of the 8bp duplication mutation in the SLC4A11 gene causing corneal dystrophy and perceptive deafness in three South American families.
Ophthalmic Genet
; 40(2): 91-98, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30856043
2.
Epigenetic alterations related to early-life stressful events.
Acta Neuropsychiatr
; 24(5): 255-65, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25286990