Moderation of hemophilia a phenotype by the factor v r506q mutation (1996)
- Authors:
- Autor USP: FIGUEIREDO, MAURO SILVERIO - FMRP
- Unidade: FMRP
- Assunto: DOENÇAS HEMATOLÓGICAS
- Language: Inglês
- Imprenta:
- Source:
- Título: Blood
- Volume/Número/Paginação/Ano: v.88, p.1183-7, 1996
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ABNT
NICHOLS, W C et al. Moderation of hemophilia a phenotype by the factor v r506q mutation. Blood, v. 88, p. 1183-7, 1996Tradução . . Acesso em: 01 jan. 2026. -
APA
Nichols, W. C., Amano, K., Cacheris, P. M., Figueiredo, M. S., Michaelides, K., Schwaab, R., et al. (1996). Moderation of hemophilia a phenotype by the factor v r506q mutation. Blood, 88, 1183-7. -
NLM
Nichols WC, Amano K, Cacheris PM, Figueiredo MS, Michaelides K, Schwaab R, Hoyer L, Kaufman RJ, Ginsburg D. Moderation of hemophilia a phenotype by the factor v r506q mutation. Blood. 1996 ;88 1183-7.[citado 2026 jan. 01 ] -
Vancouver
Nichols WC, Amano K, Cacheris PM, Figueiredo MS, Michaelides K, Schwaab R, Hoyer L, Kaufman RJ, Ginsburg D. Moderation of hemophilia a phenotype by the factor v r506q mutation. Blood. 1996 ;88 1183-7.[citado 2026 jan. 01 ] - Novel and recurrent mutations of factor ix gene in brazilian hemophilia b patients
- Genes dos fatores viii e ix da coagulação . Hemofilias
- Molecular analysis of hemophilia b in brazilian patients
- Haemophilia b liverpol: a new british family with mild haemophilia b associated with a -6 g to a mutation in the factor ix promotor
- High frequence of the - 6g to a factor ix promoter mutation is the result of both a founder effect and recurrent mutation at a crg dinucleotide
- Cis - acting elements and transcription factors involved in the promoter activity of the human factor viii gene
- Four novel and six recurrent mutations in brazilian hemophilia b patients
- Haemophilia B: database of point mutations and short additions and deletions, 7th edition
- Genes dos fatores viii e ix da coagulacao: mutacoes, polimorfismos e controle da expressao genica
- Transcription factor and cis-acting elements involved in the promoter activity of the human factor viii gene
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