Rhabdomyolysis: a genetic perspective (2015)
- Authors:
- Autor USP: ZANOTELI, EDMAR - FM
- Unidade: FM
- DOI: 10.1186/s13023-015-0264-3
- Subjects: FENÓTIPOS; DOENÇAS HEREDITÁRIAS (GENÉTICA); POLIMORFISMO; RHACOPHORIDAE
- Language: Inglês
- Imprenta:
- Source:
- Título: Orphanet Journal of Rare Diseases
- ISSN: 1750-1172
- Volume/Número/Paginação/Ano: v. 10, 15 p., art. 51, 2015
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
ABNT
SCALCO, Renata Siciliani et al. Rhabdomyolysis: a genetic perspective. Orphanet Journal of Rare Diseases, v. 10, p. 15 , 2015Tradução . . Disponível em: https://doi.org/10.1186/s13023-015-0264-3. Acesso em: 30 dez. 2025. -
APA
Scalco, R. S., Gardiner, A. R., Pitceathly, R. D. S., Zanoteli, E., Becker, J., Holton, J. L., et al. (2015). Rhabdomyolysis: a genetic perspective. Orphanet Journal of Rare Diseases, 10, 15 . doi:10.1186/s13023-015-0264-3 -
NLM
Scalco RS, Gardiner AR, Pitceathly RDS, Zanoteli E, Becker J, Holton JL, Houlden H, Jungbluth H, Quinlivan R. Rhabdomyolysis: a genetic perspective [Internet]. Orphanet Journal of Rare Diseases. 2015 ; 10 15 .[citado 2025 dez. 30 ] Available from: https://doi.org/10.1186/s13023-015-0264-3 -
Vancouver
Scalco RS, Gardiner AR, Pitceathly RDS, Zanoteli E, Becker J, Holton JL, Houlden H, Jungbluth H, Quinlivan R. Rhabdomyolysis: a genetic perspective [Internet]. Orphanet Journal of Rare Diseases. 2015 ; 10 15 .[citado 2025 dez. 30 ] Available from: https://doi.org/10.1186/s13023-015-0264-3 - Myopathy due to HMGCR antibodies in adult mimicking muscular dystrophy associated with cancer and statin exposure - narrative review of the literature - case report
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Informações sobre o DOI: 10.1186/s13023-015-0264-3 (Fonte: oaDOI API)
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