A phenylalanine Hydroxylase amino acid polymorphism with implications for meolecular diagnostics (2001)
- Authors:
- Autor USP: ZAGO, MARCO ANTONIO - FMRP
- Unidade: FMRP
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Molecular Genetics and Metabolism
- ISSN: 1096-7192
- Volume/Número/Paginação/Ano: v. 73, p. 280-284, 2001
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ABNT
GJETTING, Torben et al. A phenylalanine Hydroxylase amino acid polymorphism with implications for meolecular diagnostics. Molecular Genetics and Metabolism, v. 73, p. 280-284, 2001Tradução . . Acesso em: 20 abr. 2024. -
APA
Gjetting, T., Romstad, A., Haavik, J., Knappskog, P. M., Acosta, A. X., Silva Júnior, W. A. da, et al. (2001). A phenylalanine Hydroxylase amino acid polymorphism with implications for meolecular diagnostics. Molecular Genetics and Metabolism, 73, 280-284. -
NLM
Gjetting T, Romstad A, Haavik J, Knappskog PM, Acosta AX, Silva Júnior WA da, Zago MA, Guldberg P, Güttler F. A phenylalanine Hydroxylase amino acid polymorphism with implications for meolecular diagnostics. Molecular Genetics and Metabolism. 2001 ; 73 280-284.[citado 2024 abr. 20 ] -
Vancouver
Gjetting T, Romstad A, Haavik J, Knappskog PM, Acosta AX, Silva Júnior WA da, Zago MA, Guldberg P, Güttler F. A phenylalanine Hydroxylase amino acid polymorphism with implications for meolecular diagnostics. Molecular Genetics and Metabolism. 2001 ; 73 280-284.[citado 2024 abr. 20 ] - Trombofilia em pacientes jovens com acidente vascular cerebral isquêmico (AVCI)
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