Haemophilia B: database of point mutations and short additions and deletions, 7th edition (1997)
- Authors:
- Autor USP: FIGUEIREDO, MAURO SILVERIO - FMRP
- Unidade: FMRP
- DOI: 10.1093/nar/26.1.265
- Subjects: HEMATOLOGIA; GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Nucleic Acids Research
- Volume/Número/Paginação/Ano: v. 25, n. 1, p. 175-177, 1997
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
GIANELLI, F et al. Haemophilia B: database of point mutations and short additions and deletions, 7th edition. Nucleic Acids Research, v. 25, n. 1, p. 175-177, 1997Tradução . . Disponível em: https://doi.org/10.1093/nar/26.1.265. Acesso em: 31 dez. 2025. -
APA
Gianelli, F., Green, P. M., Sommer, S. S., Poon, M. -C., Ludwig, M., Schwaab, R., et al. (1997). Haemophilia B: database of point mutations and short additions and deletions, 7th edition. Nucleic Acids Research, 25( 1), 175-177. doi:10.1093/nar/26.1.265 -
NLM
Gianelli F, Green PM, Sommer SS, Poon M-C, Ludwig M, Schwaab R, Reitsma PH, Goossens M, Yoshioka A, Figueiredo MS, Brownlee GG. Haemophilia B: database of point mutations and short additions and deletions, 7th edition [Internet]. Nucleic Acids Research. 1997 ; 25( 1): 175-177.[citado 2025 dez. 31 ] Available from: https://doi.org/10.1093/nar/26.1.265 -
Vancouver
Gianelli F, Green PM, Sommer SS, Poon M-C, Ludwig M, Schwaab R, Reitsma PH, Goossens M, Yoshioka A, Figueiredo MS, Brownlee GG. Haemophilia B: database of point mutations and short additions and deletions, 7th edition [Internet]. Nucleic Acids Research. 1997 ; 25( 1): 175-177.[citado 2025 dez. 31 ] Available from: https://doi.org/10.1093/nar/26.1.265 - 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
- Moderation of hemophilia a phenotype by the factor v r506q mutation
- 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
- 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
Informações sobre o DOI: 10.1093/nar/26.1.265 (Fonte: oaDOI API)
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