Santos syndrome is caused by mutation in the WNT7A gene (2017)
- Authors:
- Autor USP: KOK, FERNANDO - FM
- Unidade: FM
- DOI: 10.1038/jhg.2017.86
- Subjects: MUTAÇÃO GENÉTICA; SEQUENCIAMENTO GENÉTICO; DOENÇAS GENÉTICAS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of human genetics
- ISSN: 1434-5161
- Volume/Número/Paginação/Ano: v. 62, n. 12, p. 1073-1078, 2017
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
ALVES, Leandro U. et al. Santos syndrome is caused by mutation in the WNT7A gene. Journal of human genetics, v. 62, n. 12, p. 1073-1078, 2017Tradução . . Disponível em: https://doi.org/10.1038/jhg.2017.86. Acesso em: 26 jan. 2026. -
APA
Alves, L. U., Santos, S., Musso, C. M., Ezquina, S. A. M., Opitz, J. M., Kok, F., et al. (2017). Santos syndrome is caused by mutation in the WNT7A gene. Journal of human genetics, 62( 12), 1073-1078. doi:10.1038/jhg.2017.86 -
NLM
Alves LU, Santos S, Musso CM, Ezquina SAM, Opitz JM, Kok F, Otto PA, Mingroni Netto RC. Santos syndrome is caused by mutation in the WNT7A gene [Internet]. Journal of human genetics. 2017 ; 62( 12): 1073-1078.[citado 2026 jan. 26 ] Available from: https://doi.org/10.1038/jhg.2017.86 -
Vancouver
Alves LU, Santos S, Musso CM, Ezquina SAM, Opitz JM, Kok F, Otto PA, Mingroni Netto RC. Santos syndrome is caused by mutation in the WNT7A gene [Internet]. Journal of human genetics. 2017 ; 62( 12): 1073-1078.[citado 2026 jan. 26 ] Available from: https://doi.org/10.1038/jhg.2017.86 - Heterozygous loss of function of NR4A2 is associated with intellectual deficiency, rolandic epilepsy, and language impairment
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Informações sobre o DOI: 10.1038/jhg.2017.86 (Fonte: oaDOI API)
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