2q24.2 microdeletions encompassing the SLC4A10 gene are associated with idiopathic epilepsy and mental impairment (2009)
- Authors:
- USP affiliated authors: BERTOLA, DÉBORA ROMEO - IB ; MORGANTE, ANGELA MARIA VIANNA - IB
- Unidade: IB
- Assunto: RETARDO MENTAL
- Language: Inglês
- Imprenta:
- Source:
- Título: Abstracts
- Conference titles: International Workshop on Fragile X and X-Linked Mental Retardation
-
ABNT
KREPISCHI, Ana Cristina Victorino et al. 2q24.2 microdeletions encompassing the SLC4A10 gene are associated with idiopathic epilepsy and mental impairment. 2009, Anais.. Salvador: Instituto de Biociências, Universidade de São Paulo, 2009. . Acesso em: 27 dez. 2025. -
APA
Krepischi, A. C. V., Knijnenburg, J., Bertola, D. R., Kim, C. A., Kok, F., Vianna-Morgante, A. M., & Rosenberg, C. (2009). 2q24.2 microdeletions encompassing the SLC4A10 gene are associated with idiopathic epilepsy and mental impairment. In Abstracts. Salvador: Instituto de Biociências, Universidade de São Paulo. -
NLM
Krepischi ACV, Knijnenburg J, Bertola DR, Kim CA, Kok F, Vianna-Morgante AM, Rosenberg C. 2q24.2 microdeletions encompassing the SLC4A10 gene are associated with idiopathic epilepsy and mental impairment. Abstracts. 2009 ;[citado 2025 dez. 27 ] -
Vancouver
Krepischi ACV, Knijnenburg J, Bertola DR, Kim CA, Kok F, Vianna-Morgante AM, Rosenberg C. 2q24.2 microdeletions encompassing the SLC4A10 gene are associated with idiopathic epilepsy and mental impairment. Abstracts. 2009 ;[citado 2025 dez. 27 ] - Duplication restricted to ICR2 (KCNQ1, KCNQ1OT1 genes) at 11p15 segregating in a family with five children affected by Silver-Russel syndrome
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- Estudo do gene PTPN11 nos pacientes afetados pela síndrome de Noonan
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