SHARMA, N.; DANTALIYA, U. A rare case of spondyloepimetaphyseal dysplasia with joint laxity, type 3 (EXOC6B gene) (SEMDJL3). International Journal of Contemporary Pediatrics, [S. l.], v. 13, n. 7, p. 1256–1259, 2026. DOI: 10.18203/2349-3291.ijcp20261924. Disponível em: https://www.ijpediatrics.com/index.php/ijcp/article/view/7526. Acesso em: 23 jun. 2026.