Lipoid proteinosis: Rare case confirmed by ECM1 mutation detection (2014)
Source: International Journal of Pediatric Otorhinolaryngology. Unidades: FM, IB
Subjects: MANIFESTAÇÕES CUTÂNEAS, MUTAÇÃO GENÉTICA, PROGNÓSTICO, DERMATOPATIAS
ABNT
ALMEIDA, Tatiana F. et al. Lipoid proteinosis: Rare case confirmed by ECM1 mutation detection. International Journal of Pediatric Otorhinolaryngology, v. 78, p. 2314-2315, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.ijporl.2014.09.025. Acesso em: 28 out. 2024.APA
Almeida, T. F., Soares, D. C., Quaio, C. R., Honjo, R. S., Bertola, D. R., McGrath, J. A., & Kim, C. A. (2014). Lipoid proteinosis: Rare case confirmed by ECM1 mutation detection. International Journal of Pediatric Otorhinolaryngology, 78, 2314-2315. doi:10.1016/j.ijporl.2014.09.025NLM
Almeida TF, Soares DC, Quaio CR, Honjo RS, Bertola DR, McGrath JA, Kim CA. Lipoid proteinosis: Rare case confirmed by ECM1 mutation detection [Internet]. International Journal of Pediatric Otorhinolaryngology. 2014 ; 78 2314-2315.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.ijporl.2014.09.025Vancouver
Almeida TF, Soares DC, Quaio CR, Honjo RS, Bertola DR, McGrath JA, Kim CA. Lipoid proteinosis: Rare case confirmed by ECM1 mutation detection [Internet]. International Journal of Pediatric Otorhinolaryngology. 2014 ; 78 2314-2315.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.ijporl.2014.09.025