Mutational analysis of mitochondrial tRNA genes in 138 patients with Leber's hereditary optic neuropathy.

Shuai, Jie; Shi, Jian; Liang, Ya; Ji, Fangfang; Gu, Luo; Yuan, Zhilan

Shuai, Jie; Shi, Jian; Liang, Ya; Ji, Fangfang; Gu, Luo; Yuan, Zhilan.

Afiliación

Shuai J; Department of Ophthalmology, the Affiliated Hospital of Nantong University, Nantong, China.
Shi J; Department of Ophthalmology, the Affiliated Hospital of Nantong University, Nantong, China.
Liang Y; Department of Ophthalmology, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, Jiangsu Province, China.
Ji F; Department of Ophthalmology, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, Jiangsu Province, China.
Gu L; Department of Physiology, Nanjing Medical University, Nanjing, China.
Yuan Z; Department of Ophthalmology, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, Jiangsu Province, China. yuanzhilan001@sohu.com.

Ir J Med Sci ; 191(2): 865-876, 2022 Apr.

Article en En | MEDLINE | ID: mdl-34053002

Asunto(s)

Atrofia Óptica Hereditaria de Leber; ADN Mitocondrial/genética; Humanos; Mutación; Atrofia Óptica Hereditaria de Leber/genética; Atrofia Óptica Hereditaria de Leber/patología; Filogenia; ARN de Transferencia/genética

Palabras clave

LHON; Mitochondrial dysfunction; Mt-tRNA; Pathogenic; Variants

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Atrofia Óptica Hereditaria de Leber Tipo de estudio: Prognostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Ir J Med Sci Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Irlanda

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