Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals (2023)
- Authors:
- Autor USP: KIM, CHONG AE - FM
- Unidade: FM
- DOI: 10.1016/j.gim.2022.09.010
- Subjects: AGENTES DOPAMINÉRGICOS; CÉREBRO
- Agências de fomento:
- Financiamento AMED
- Financiamento JSPS
- Financiamento Takeda Science Foundation
- Financiamento NHLBI
- Financiamento National Institute of Neurological Disorders and Stroke
- Financiamento Muscular Dystrophy Association
- Financiamento NIH
- Financiamento American Brain Foundation
- Financiamento Muscle Study Group
- Financiamento Rett Syndrome Foundation
- Financiamento NHGRI/NIH
- Financiamento Medical Research Council, UK
- Financiamento UCLH-BRC/NIHR
- Financiamento Rosetree Trust
- Financiamento Ataxia UK
- Financiamento Multiple System Atrophy Trust
- Financiamento Brain Research UK
- Financiamento GOSH
- Financiamento Muscular Dystrophy UK
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Genetics in medicine
- ISSN: 1098-3600
- Volume/Número/Paginação/Ano: v. 25, n. 1, p. 90-102, 2023
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: green
- Licença: publisher-specific-oa
-
ABNT
SAIDA, Ken et al. Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals. Genetics in medicine, v. 25, n. 1, p. 90-102, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/53033. Acesso em: 28 abr. 2024. -
APA
Saida, K., Marootain, R., Sengoku, T., Mitani, T., Pagnamenta, A. T., Marafi, D., et al. (2023). Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals. Genetics in medicine, 25( 1), 90-102. doi:10.1016/j.gim.2022.09.010 -
NLM
Saida K, Marootain R, Sengoku T, Mitani T, Pagnamenta AT, Marafi D, Zaki MS, O'Brien TJ, Karimiani EG, Kaiyrzhanov R, Ceroni JRM, Kim CA. Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals [Internet]. Genetics in medicine. 2023 ; 25( 1): 90-102.[citado 2024 abr. 28 ] Available from: https://observatorio.fm.usp.br/handle/OPI/53033 -
Vancouver
Saida K, Marootain R, Sengoku T, Mitani T, Pagnamenta AT, Marafi D, Zaki MS, O'Brien TJ, Karimiani EG, Kaiyrzhanov R, Ceroni JRM, Kim CA. Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals [Internet]. Genetics in medicine. 2023 ; 25( 1): 90-102.[citado 2024 abr. 28 ] Available from: https://observatorio.fm.usp.br/handle/OPI/53033 - Caracterização clínico-laboratorial das Síndromes de Williams-Beuren e de Noonan
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Informações sobre o DOI: 10.1016/j.gim.2022.09.010 (Fonte: oaDOI API)
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