Detalhe da pesquisa
1.
Ceramide synthase TLCD3B is a novel gene associated with human recessive retinal dystrophy.
Genet Med
; 23(3): 488-497, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33077892
2.
Molecular Screening of 43 Brazilian Families Diagnosed with Leber Congenital Amaurosis or Early-Onset Severe Retinal Dystrophy.
Genes (Basel)
; 8(12)2017 Nov 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-29186038