Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
---|---|---|---|
1 |
Material Type: Artigo
|
![]() |
Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delayUirá Souto Melo Devon Bonner; Kevin C. Kent Lloyd; Ala Moshiri; Brandon Willis; Louise Lanoue; Lynette Bower; Brian C Leonard; Davi Jardim Martins; Fernando Gomes; Felipe de Souza Leite; Danyllo Oliveira Danyllo Felipe de Oliveira; João Paulo Kitajima Joao Paulo Fumio Whitaker Kitajima; Fabiola P Monteiro Fabiola Paoli Mendes Monteiro; Mayana Zatz; Carlos Frederico Martins Menck; Matthew T Wheeler; Jonathan A Bernstein; Kevin Dumas; Elizabeth Spiteri; Nataliya Di Donato; Arne Jahn; Mais Hashem Mais Omar Hashem; Hessa S Alsaif; Aziza Chedrawi Aziza K. Chedrawi; Fowzan S Alkuraya; Fernando Kok; Heather M ByersGenetics in Medicine Philadelphia v. 23, n. 4, p. 6611-668, 2021Philadelphia 2021Item não circula. Consulte sua biblioteca.(Acessar) |
2 |
Material Type: Artigo
|
![]() |
Expanding the clinical and genetic spectrum of CAD deficiency: an epileptic encephalopathy treatable with uridine supplementationRymen, Daisy ; Lindhout, Martijn ; Spanou, Maria ; Ashrafzadeh, Farah ; Benkel, Ira ; Betzler, Cornelia ; Coubes, Christine ; Hartmann, Hans ; Kaplan, Julie D ; Ballhausen, Diana ; Koch, Johannes ; Lotte, Jan ; Mohammadi, Mohammad Hasan ; Rohrbach, Marianne ; Dinopoulos, Argirios ; Wermuth, Marieke ; Willis, Daniel ; Brugger, Karin ; Wevers, Ron A ; Boltshauser, Eugen ; Bierau, Jorgen ; Mayr, Johannes A ; Wortmann, Saskia BGENETICS IN MEDICINE, 2020-10, Vol.22 (10), p.1589-1597 [Periódico revisado por pares]ELSEVIER SCIENCE INCTexto completo disponível |