Detalhe da pesquisa
1.
A Recurrent Nonsense Mutation in NECTIN4 Underlying Ectodermal Dysplasia-Syndactyly Syndrome with a Novel Phenotype in a Consanguineous Kashmiri Family.
Genet Res (Camb)
; 2023: 9999660, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37829154