Human prion protein gene mutation at codon 183 associated with an atypical form of prion disease (1998)
- Authors:
- USP affiliated authors: NITRINI, RICARDO - FM ; ROSEMBERG, SERGIO - FM ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidades: FM; IB
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Publisher: Plenum Press
- Publisher place: New York
- Date published: 1998
- Source:
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ABNT
NITRINI, Ricardo et al. Human prion protein gene mutation at codon 183 associated with an atypical form of prion disease. Prions and brain diseases in animals and humans. Tradução . New York: Plenum Press, 1998. . . Acesso em: 02 maio 2025. -
APA
Nitrini, R., Rosemberg, S., Passos-Bueno, M. R., Silva, L. S. T., Iughetti, P., Papadopoulos, M., et al. (1998). Human prion protein gene mutation at codon 183 associated with an atypical form of prion disease. In Prions and brain diseases in animals and humans. New York: Plenum Press. -
NLM
Nitrini R, Rosemberg S, Passos-Bueno MR, Silva LST, Iughetti P, Papadopoulos M, Carrilho PM, Caramelli P, Albrecht S, Zatz M, LeBanc A. Human prion protein gene mutation at codon 183 associated with an atypical form of prion disease. In: Prions and brain diseases in animals and humans. New York: Plenum Press; 1998. [citado 2025 maio 02 ] -
Vancouver
Nitrini R, Rosemberg S, Passos-Bueno MR, Silva LST, Iughetti P, Papadopoulos M, Carrilho PM, Caramelli P, Albrecht S, Zatz M, LeBanc A. Human prion protein gene mutation at codon 183 associated with an atypical form of prion disease. In: Prions and brain diseases in animals and humans. New York: Plenum Press; 1998. [citado 2025 maio 02 ] - Fine mapping and clinical reevaluation of a Brazilian pedigree with a severe form of X-linked mental retardation associated with other neurological dysfunction
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