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Heterozygote MTHFR A1298C mutation in a case of autosomal recessive bestrophinopathy with branch retinal vein occlusion.
Hemmati, Sara; Khakpour, Golnaz; Nadjafi-Semnani, Fatemeh; Gordiz, Arzhang; Sajadi, Masoome; Abdi, Fatemeh.
Afiliação
  • Hemmati S; Eye Research Center, the Five Senses Institute, Rassoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Khakpour G; Eye Research Center, the Five Senses Institute, Rassoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Nadjafi-Semnani F; Eye Research Center, the Five Senses Institute, Rassoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Gordiz A; Eye Research Center, the Five Senses Institute, Rassoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Sajadi M; Eye Research Center, the Five Senses Institute, Rassoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Abdi F; Eye Research Center, the Five Senses Institute, Rassoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
Ophthalmic Genet ; 43(1): 140-142, 2022 02.
Article em En | MEDLINE | ID: mdl-35232319
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Oclusão da Veia Retiniana Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Ophthalmic Genet Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Oclusão da Veia Retiniana Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Ophthalmic Genet Ano de publicação: 2022 Tipo de documento: Article