Epilepsy in patients with Angelman Syndrome caused by deletion of the chromosome 15q11-13 (2006)
- Authors:
- USP affiliated authors: KOIFFMANN, CELIA PRISZKULNIK - IB ; DIAS, MARIA JOAQUINA MARQUES - FM
- Unidades: IB; FM
- Subjects: SÍNDROME DE ANGELMAN; RETARDO MENTAL SEVERO
- Language: Inglês
- Imprenta:
- Source:
- Título: Archives of Neurology
- ISSN: 0003-9942
- Volume/Número/Paginação/Ano: v. 63, n. 1, p. 122-128, 2006
-
ABNT
VALENTE, Kette D. et al. Epilepsy in patients with Angelman Syndrome caused by deletion of the chromosome 15q11-13. Archives of Neurology, v. 63, n. 1, p. 122-128, 2006Tradução . . Acesso em: 21 fev. 2026. -
APA
Valente, K. D., Koiffmann, C. P., Fridman, C., Varella, M. C., Kok, F., Andrade, J. C. Q. F. de, et al. (2006). Epilepsy in patients with Angelman Syndrome caused by deletion of the chromosome 15q11-13. Archives of Neurology, 63( 1), 122-128. -
NLM
Valente KD, Koiffmann CP, Fridman C, Varella MC, Kok F, Andrade JCQF de, Grossmann RM, Marques-Dias MJ. Epilepsy in patients with Angelman Syndrome caused by deletion of the chromosome 15q11-13. Archives of Neurology. 2006 ; 63( 1): 122-128.[citado 2026 fev. 21 ] -
Vancouver
Valente KD, Koiffmann CP, Fridman C, Varella MC, Kok F, Andrade JCQF de, Grossmann RM, Marques-Dias MJ. Epilepsy in patients with Angelman Syndrome caused by deletion of the chromosome 15q11-13. Archives of Neurology. 2006 ; 63( 1): 122-128.[citado 2026 fev. 21 ] - Angelman syndrome caused by deletion: a genotype—phenotype correlation determined by breakpoint
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