Association of CHRNA5 gene variants with crack cocaine addiction (2020)
- Authors:
- Autor USP: ROVARIS, DIEGO LUIZ - ICB
- Unidade: ICB
- DOI: 10.1007/s12017-020-08596-1
- Subjects: FISIOLOGIA; COCAÍNA CRACK; DEPENDENTES QUÍMICOS; HAPLOTIPOS; GENOMAS; VARIAÇÃO GENÉTICA; COLINÉRGICOS; POLIMORFISMO; TRANSTORNOS RELACIONADOS AO USO DE COCAÍNA; TRANSTORNOS RELACIONADOS AO USO DE SUBSTÂNCIAS; NUCLEOTÍDEOS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher place: Heidelberg
- Date published: 2020
- Source:
- Título: NeuroMolecular Medicine
- ISSN: 1559-1174
- Volume/Número/Paginação/Ano: v. 22, p. 384–390, 2020
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
AROCHE, Angelita P. et al. Association of CHRNA5 gene variants with crack cocaine addiction. NeuroMolecular Medicine, v. 22, p. 384–390, 2020Tradução . . Disponível em: https://doi.org/10.1007/s12017-020-08596-1. Acesso em: 11 fev. 2026. -
APA
Aroche, A. P., Grevet, E. H., Stolf, A. R., Vieira, B. S., Kessler, F. H. P., Diemen, L. von, et al. (2020). Association of CHRNA5 gene variants with crack cocaine addiction. NeuroMolecular Medicine, 22, 384–390. doi:10.1007/s12017-020-08596-1 -
NLM
Aroche AP, Grevet EH, Stolf AR, Vieira BS, Kessler FHP, Diemen L von, Grassi-Oliveira RG, Bau CHD, Rovaris DL. Association of CHRNA5 gene variants with crack cocaine addiction [Internet]. NeuroMolecular Medicine. 2020 ; 22 384–390.[citado 2026 fev. 11 ] Available from: https://doi.org/10.1007/s12017-020-08596-1 -
Vancouver
Aroche AP, Grevet EH, Stolf AR, Vieira BS, Kessler FHP, Diemen L von, Grassi-Oliveira RG, Bau CHD, Rovaris DL. Association of CHRNA5 gene variants with crack cocaine addiction [Internet]. NeuroMolecular Medicine. 2020 ; 22 384–390.[citado 2026 fev. 11 ] Available from: https://doi.org/10.1007/s12017-020-08596-1 - Refining patterns of MEF2C effects in white matter microstructure and psychiatric features
- Caffeine-related genes influence anxiety disorders in children and adults with ADHD
- The course of attention-deficit/hyperactivity disorder through midlife
- Emerging findings of glutamate–glutamine imbalance in the medial prefrontal cortex in attention deficit/hyperactivity disorder: systematic review and meta-analysis of spectroscopy studies
- The neurodevelopmental nature of attention-deficit hyperactivity disorder in adults
- Infantile hemangiomas: risk factors for complications, recurrence and unaesthetic sequelae
- Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p
- Expanding the discussion on experimental models of attention deficit hyperactivity disorder
- Dissecting the cross-trait effects of the FOXP2 GWAS hit on clinical and brain phenotypes in adults with ADHD
- Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders, and known risk factors
Informações sobre o DOI: 10.1007/s12017-020-08596-1 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
