A heterozygous PMP22 THR(118)MET substitution running in a family with 17PTANDEM duplication (1998)
- Authors:
- Autor USP: MARQUES JUNIOR, WILSON - FMRP
- Unidade: FMRP
- Assunto: TRANSTORNOS CEREBROVASCULARES
- Language: Inglês
- Imprenta:
- Source:
- Título: Abstracts
- Conference titles: International Conference on Charcot-Marie-Tooth Disorders
-
ABNT
MARQUES JÚNIOR, Wilson e SWEENEY, M G e WOOD, N W. A heterozygous PMP22 THR(118)MET substitution running in a family with 17PTANDEM duplication. 1998, Anais.. Quebec: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 1998. . Acesso em: 28 jan. 2026. -
APA
Marques Júnior, W., Sweeney, M. G., & Wood, N. W. (1998). A heterozygous PMP22 THR(118)MET substitution running in a family with 17PTANDEM duplication. In Abstracts. Quebec: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Marques Júnior W, Sweeney MG, Wood NW. A heterozygous PMP22 THR(118)MET substitution running in a family with 17PTANDEM duplication. Abstracts. 1998 ;[citado 2026 jan. 28 ] -
Vancouver
Marques Júnior W, Sweeney MG, Wood NW. A heterozygous PMP22 THR(118)MET substitution running in a family with 17PTANDEM duplication. Abstracts. 1998 ;[citado 2026 jan. 28 ] - Mutational analysis of LITAF, EGR2 and NEFL genes in a Brazilian population of Charcot-Marie-Tooth neuropathy type I
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