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A new phenotype of MT-ND6 gene mutation for Leber's hereditary optic neuropathy.
Lee, Chaeyeon; Jang, Ja-Hyun; Park, Kyung-Ah; Lee, Ga-In; Oh, Sei Yeul.
Afiliação
  • Lee C; Department of Ophthalmology, Samsung Medical Centre, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul, 06351, Korea.
  • Jang JH; Department of Laboratory Medicine and Genetics, Samsung Medical Centre, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Park KA; Department of Ophthalmology, Samsung Medical Centre, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul, 06351, Korea. kparkoph@skku.edu.
  • Lee GI; Department of Ophthalmology, Samsung Medical Centre, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul, 06351, Korea.
  • Oh SY; Department of Ophthalmology, Samsung Medical Centre, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul, 06351, Korea.
Neurol Sci ; 42(10): 4367-4371, 2021 Oct.
Article em En | MEDLINE | ID: mdl-34264415
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Atrofia Óptica Hereditária de Leber Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Atrofia Óptica Hereditária de Leber Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article