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A novel stop codon mutation in the PMP22 gene associated with a variable phenotype
A novel stop codon mutation in the PMP22 gene associated with a variable phenotype
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

A novel stop codon mutation in the PMP22 gene associated with a variable phenotype

Kikue Terada Abe Maria Rita Passos-Bueno; Rita de Cássia M Pavanello; A. M. M Lino; M. T. A Hirata; M.W Brotto; P. E Marchiori; Mayana Zatz; International Congress of the World Muscle Society (7. 2002 Rotterdam)

Neuromuscular Disorders v. 12, n. 7-8, p. 762-763, oct. 2002

Oxford 2002

Item não circula. Consulte sua biblioteca.(Acessar)

2
A novel stop codon mutation in the PMP22 gene associated with a variable phenotype
A novel stop codon mutation in the PMP22 gene associated with a variable phenotype
Material Type:
Artigo 		Adicionar ao Meu Espaço

A novel stop codon mutation in the PMP22 gene associated with a variable phenotype

Kikue Terada Abe A. M. M Lino; M. T. A Hirata; Rita de Cássia M Pavanello; Mário Wilson Iervolino Brotto; Paulo Eurípedes Marchiori; Mayana Zatz

Neuromuscular Disorders v. 14, n. 5, p. 313-320, 2004

Amsterdam 2004

Acesso online

3
A novel stop codon mutation in the PMP22 gene associated with a variable phenotype
A novel stop codon mutation in the PMP22 gene associated with a variable phenotype
Material Type:
Artigo 		Adicionar ao Meu Espaço

A novel stop codon mutation in the PMP22 gene associated with a variable phenotype

Kikue Terada Abe A. M. M Lino; M. T. A Hirata; Rita de Cássia M Pavanello; Mário Wilson Iervolino Brotto; Paulo Eurípedes Marchiori; Mayana Zatz

Neuromuscular Disorders v. 14, n. 5, p. 313-320, 2004

Amsterdam 2004

Acesso online

4
O.5 Skeletal muscle-specific calpain, p94/calpain 3, dynamically distributes in skeletal muscle cells to adapt to physical stress, defects of which cause muscular dystrophy
O.5 Skeletal muscle-specific calpain, p94/calpain 3, dynamically distributes in skeletal muscle cells to adapt to physical stress, defects of which cause muscular dystrophy
Material Type:
Artigo 		Adicionar ao Meu Espaço

O.5 Skeletal muscle-specific calpain, p94/calpain 3, dynamically distributes in skeletal muscle cells to adapt to physical stress, defects of which cause muscular dystrophy

Ojima, K ; Ono, Y ; Doi, N ; Kitamura, F ; Hata, S ; Kawabata, Y ; Suzuki, K ; Maeda, T ; Abe, K ; Nakao, H ; Aiba, A ; Nakao, K ; Suzuki, H ; Kawahara, H ; Witt, C ; Labeit, S ; Ottenheijm, C ; Granzier, H ; Toyama-Sorimachi, N ; Sorimachi, M ; Sorimachi, H

Neuromuscular disorders : NMD, 2010-10, Vol.20 (9), p.598-599 [Periódico revisado por pares]

Elsevier B.V

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Deste Autor:

  1. Hirata, M
  2. Marchiori, P
  3. Brotto, M
  4. Pavanello, R
  5. Lino, A

Neste Assunto:

  1. Distrofia Muscular
  2. Doenças Genéticas
  3. Mutação Genética
  4. Eletrofisiologia
  5. Neurology

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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