Mucopolysaccharidosis Type IVA: Evidence of Primary and Secondary Central Nervous System Involvement (2014)
- Authors:
- USP affiliated authors: BERTOLA, DÉBORA ROMEO - IB ; KIM, CHONG AE - FM
- Unidades: IB; FM
- DOI: 10.1002/ajmg.a.36424
- Subjects: SISTEMA NERVOSO CENTRAL; ESQUELETO (ANORMALIDADES); GLICOSAMINOGLICANAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American journal of medical genetics part. A
- ISSN: 1552-4825
- Volume/Número/Paginação/Ano: v. 164A, n. 5, p. 1162\20131169, 2014
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
BORLOT, Felippe et al. Mucopolysaccharidosis Type IVA: Evidence of Primary and Secondary Central Nervous System Involvement. American journal of medical genetics part. A, v. 164A, n. 5, p. 1162\20131169, 2014Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.36424/pdf. Acesso em: 19 abr. 2024. -
APA
Borlot, F., Arantes, P. R., Quaio, C. R., Franco, J. F. da S., Lourenço, C. M., Gomy, I., et al. (2014). Mucopolysaccharidosis Type IVA: Evidence of Primary and Secondary Central Nervous System Involvement. American journal of medical genetics part. A, 164A( 5), 1162\20131169. doi:10.1002/ajmg.a.36424 -
NLM
Borlot F, Arantes PR, Quaio CR, Franco JF da S, Lourenço CM, Gomy I, Bertola DR, Kim CA. Mucopolysaccharidosis Type IVA: Evidence of Primary and Secondary Central Nervous System Involvement [Internet]. American journal of medical genetics part. A. 2014 ; 164A( 5): 1162\20131169.[citado 2024 abr. 19 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.36424/pdf -
Vancouver
Borlot F, Arantes PR, Quaio CR, Franco JF da S, Lourenço CM, Gomy I, Bertola DR, Kim CA. Mucopolysaccharidosis Type IVA: Evidence of Primary and Secondary Central Nervous System Involvement [Internet]. American journal of medical genetics part. A. 2014 ; 164A( 5): 1162\20131169.[citado 2024 abr. 19 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.36424/pdf - Clinical description of 41 Brazilian patients with oculo-auriculo-vertebral dysplasia
- Displasias esqueléticas
- Patients with a Kabuki syndrome phenotype demonstrate DNA methylation abnormalities
- New insight in mucopolysaccharidosis type VI: Neurological perspective
- New Insights in mucopolysaccharidosis type VI: Neurological perspective
- Síndromes genéticas associadas à obesidade
- Lipoid proteinosis: Rare case confirmed by ECM1 mutation detection
- Multicentric study on the diagnosis of Fabry's disease using angiokeratoma biopsy registries [Carta]
- Cytogenomic delineation and clinical follow-up of 10 Brazilian patients with Pallister-Killian syndrome
- Abordagem genético-clínica na síndrome de Down
Informações sobre o DOI: 10.1002/ajmg.a.36424 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
