SMN1 gene study for diagnosis of spinal muscular atrophy (SMA) (2010)
- Authors:
- USP affiliated authors: REED, UMBERTINA CONTI - FM ; CHADI, GERSON - FM
- Unidade: FM
- Subjects: ATROFIA MUSCULAR (DIAGNÓSTICO;GENÉTICA); GENES (ANÁLISE); DOENÇAS NEUROMUSCULARES; REAÇÃO EM CADEIA POR POLIMERASE; DELEÇÃO DE GENES; RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Source:
- Conference titles: Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP"
-
ABNT
PASQUALIN, L M A et al. SMN1 gene study for diagnosis of spinal muscular atrophy (SMA). Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 15 nov. 2024. , 2010 -
APA
Pasqualin, L. M. A., Pieri, P. C., Resende, M. B. D., Xavier, G. O., Campos, E. D., Reed, U. C., et al. (2010). SMN1 gene study for diagnosis of spinal muscular atrophy (SMA). Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Pasqualin LMA, Pieri PC, Resende MBD, Xavier GO, Campos ED, Reed UC, Chadi G, Zanoteli E. SMN1 gene study for diagnosis of spinal muscular atrophy (SMA). Clinics. 2010 ; 65 S77.[citado 2024 nov. 15 ] -
Vancouver
Pasqualin LMA, Pieri PC, Resende MBD, Xavier GO, Campos ED, Reed UC, Chadi G, Zanoteli E. SMN1 gene study for diagnosis of spinal muscular atrophy (SMA). Clinics. 2010 ; 65 S77.[citado 2024 nov. 15 ] - Duchenne muscular dystrophy and Duane's syndrome: a rare association [Carta]
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