Identification of five novel mutations in brazilian families with X-linked CMT (2017)
- Authors:
- Autor USP: MARQUES JÚNIOR, WILSON - FMRP
- Unidade: FMRP
- Subjects: MUTAÇÃO GENÉTICA; FENÓTIPOS; DOENÇAS DO SISTEMA NERVOSO
- Language: Inglês
- Imprenta:
- Source:
- Título: Abstracts
- Conference titles: Annual Meeting of Peripheral Nerve Society - PNS
-
ABNT
TOMASELLI, P. J. et al. Identification of five novel mutations in brazilian families with X-linked CMT. 2017, Anais.. Barcelona: PNS, 2017. . Acesso em: 10 jan. 2026. -
APA
Tomaselli, P. J., Gouvea, S. P., Nyshyama, K. F. S., Nicolau Júnior, N., Lourenço, C. M., & Marques Júnior, W. (2017). Identification of five novel mutations in brazilian families with X-linked CMT. In Abstracts. Barcelona: PNS. -
NLM
Tomaselli PJ, Gouvea SP, Nyshyama KFS, Nicolau Júnior N, Lourenço CM, Marques Júnior W. Identification of five novel mutations in brazilian families with X-linked CMT. Abstracts. 2017 ;[citado 2026 jan. 10 ] -
Vancouver
Tomaselli PJ, Gouvea SP, Nyshyama KFS, Nicolau Júnior N, Lourenço CM, Marques Júnior W. Identification of five novel mutations in brazilian families with X-linked CMT. Abstracts. 2017 ;[citado 2026 jan. 10 ] - Mutational analysis of LITAF, EGR2 and NEFL genes in a Brazilian population of Charcot-Marie-Tooth neuropathy type I
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