Multimodal image analysis of the retina in Hunter syndrome (mucopolysaccharidosis type II): Case report (2018)
- Authors:
- Autor USP: KIM, CHONG AE - FM
- Unidade: FM
- DOI: 10.1080/13816810.2017.1354383
- Subjects: RETINA; GENÉTICA; NERVO ÓPTICO; ELETROFISIOLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: Philadelphia
- Date published: 2018
- Source:
- Título: Ophthalmic genetics
- ISSN: 1381-6810
- Volume/Número/Paginação/Ano: v. 39, n. 1, p. 103-107, 2018
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
SALVUCCI, Isadora Darriba Macedo e KIM, Chong Ae. Multimodal image analysis of the retina in Hunter syndrome (mucopolysaccharidosis type II): Case report. Ophthalmic genetics, v. 39, n. 1, p. 103-107, 2018Tradução . . Disponível em: https://doi.org/10.1080/13816810.2017.1354383. Acesso em: 28 fev. 2026. -
APA
Salvucci, I. D. M., & Kim, C. A. (2018). Multimodal image analysis of the retina in Hunter syndrome (mucopolysaccharidosis type II): Case report. Ophthalmic genetics, 39( 1), 103-107. doi:10.1080/13816810.2017.1354383 -
NLM
Salvucci IDM, Kim CA. Multimodal image analysis of the retina in Hunter syndrome (mucopolysaccharidosis type II): Case report [Internet]. Ophthalmic genetics. 2018 ; 39( 1): 103-107.[citado 2026 fev. 28 ] Available from: https://doi.org/10.1080/13816810.2017.1354383 -
Vancouver
Salvucci IDM, Kim CA. Multimodal image analysis of the retina in Hunter syndrome (mucopolysaccharidosis type II): Case report [Internet]. Ophthalmic genetics. 2018 ; 39( 1): 103-107.[citado 2026 fev. 28 ] Available from: https://doi.org/10.1080/13816810.2017.1354383 - NK and B cell deficiency in a MPS type II family with novel mutation in the IDS gene
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Informações sobre o DOI: 10.1080/13816810.2017.1354383 (Fonte: oaDOI API)
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