A novel stop codon mutation in the PMP22 gene associated with a variable phenotype (2002)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- Subjects: DISTROFIA MUSCULAR; DOENÇAS GENÉTICAS
- Language: Inglês
- Imprenta:
- Source:
- Título: Neuromuscular Disorders
- Volume/Número/Paginação/Ano: v. 12, n. 7-8, p. 762-763, oct. 2002
- Conference titles: International Congress of the World Muscle Society
-
ABNT
ABE, Kikue Terada et al. A novel stop codon mutation in the PMP22 gene associated with a variable phenotype. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 28 dez. 2025. , 2002 -
APA
Abe, K. T., Passos-Bueno, M. R., Pavanello, R. de C. M., Lino, A. M. M., Hirata, M. T. A., Brotto, M. W., et al. (2002). A novel stop codon mutation in the PMP22 gene associated with a variable phenotype. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. -
NLM
Abe KT, Passos-Bueno MR, Pavanello R de CM, Lino AMM, Hirata MTA, Brotto MW, Marchiori PE, Zatz M. A novel stop codon mutation in the PMP22 gene associated with a variable phenotype. Neuromuscular Disorders. 2002 ; 12( 7-8): 762-763.[citado 2025 dez. 28 ] -
Vancouver
Abe KT, Passos-Bueno MR, Pavanello R de CM, Lino AMM, Hirata MTA, Brotto MW, Marchiori PE, Zatz M. A novel stop codon mutation in the PMP22 gene associated with a variable phenotype. Neuromuscular Disorders. 2002 ; 12( 7-8): 762-763.[citado 2025 dez. 28 ] - Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population
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