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Phenotypic variability of SLC7A14 mutations in patients with inherited retinal dystrophy.
Guo, Li-Yun; Zheng, Sui-Lian; Li, Jun; Zhu, Qin; Duan, Wen-Hua; Zhang, Yuan; Zhu, Ying-Ting; Hu, Min.
Afiliación
  • Guo LY; a Department of Ophthalmology, the Second People's Hospital of Yunnan Province , Kunming , China.
  • Zheng SL; b Key Laboratory of Yunnan Province for the Prevention and Treatment of ophthalmology , Kunming , China.
  • Li J; c Department of Ophthalmology , Fourth Affiliated Hospital of Kunming Medical University , Kunming , China.
  • Zhu Q; d Department of Ophthalmology, the Second Affiliated Hospital , Wenzhou Medical University , Wenzhou , China.
  • Duan WH; a Department of Ophthalmology, the Second People's Hospital of Yunnan Province , Kunming , China.
  • Zhang Y; b Key Laboratory of Yunnan Province for the Prevention and Treatment of ophthalmology , Kunming , China.
  • Zhu YT; c Department of Ophthalmology , Fourth Affiliated Hospital of Kunming Medical University , Kunming , China.
  • Hu M; a Department of Ophthalmology, the Second People's Hospital of Yunnan Province , Kunming , China.
Ophthalmic Genet ; 40(2): 118-123, 2019 04.
Article en En | MEDLINE | ID: mdl-30924391
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Retinitis Pigmentosa / Mutación Missense / Sistema de Transporte de Aminoácidos y/ / Amaurosis Congénita de Leber Tipo de estudio: Prognostic_studies Límite: Female / Humans Idioma: En Revista: Ophthalmic Genet Asunto de la revista: GENETICA MEDICA / OFTALMOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Retinitis Pigmentosa / Mutación Missense / Sistema de Transporte de Aminoácidos y/ / Amaurosis Congénita de Leber Tipo de estudio: Prognostic_studies Límite: Female / Humans Idioma: En Revista: Ophthalmic Genet Asunto de la revista: GENETICA MEDICA / OFTALMOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido