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[Phenotype-genotype correlations in patients with inherited retinal diseases with p.G1961E mutation in the ABCA4 gene]. / Kliniko-geneticheskie korreliatsii u patsientov s nasledstvennymi zabolevaniiami setchatki pri mutatsii p.G1961E v gene AVSA4.
Sheremet, N L; Grushke, I G; Zhorzholadze, N V; Ronzina, I A; Mikaelyan, A A; Kadyshev, V V; Tanas, A S; Anoshkin, K I; Strelnikov, V V.
Afiliação
  • Sheremet NL; Research Institute of Eye Diseases, 11A Rossolimo St., Moscow, Russian Federation, 119021.
  • Grushke IG; Research Institute of Eye Diseases, 11A Rossolimo St., Moscow, Russian Federation, 119021.
  • Zhorzholadze NV; Research Institute of Eye Diseases, 11A Rossolimo St., Moscow, Russian Federation, 119021.
  • Ronzina IA; Research Institute of Eye Diseases, 11A Rossolimo St., Moscow, Russian Federation, 119021.
  • Mikaelyan AA; Research Institute of Eye Diseases, 11A Rossolimo St., Moscow, Russian Federation, 119021.
  • Kadyshev VV; Research Centre for Medical Genetics, 1 Moskvorech'e St., Moscow, Russian Federation, 115522.
  • Tanas AS; Research Centre for Medical Genetics, 1 Moskvorech'e St., Moscow, Russian Federation, 115522.
  • Anoshkin KI; Research Centre for Medical Genetics, 1 Moskvorech'e St., Moscow, Russian Federation, 115522.
  • Strelnikov VV; Research Centre for Medical Genetics, 1 Moskvorech'e St., Moscow, Russian Federation, 115522.
Vestn Oftalmol ; 135(4): 10-18, 2019.
Article em Ru | MEDLINE | ID: mdl-31573552

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Transportadores de Cassetes de Ligação de ATP / Degeneração Macular Limite: Humans Idioma: Ru Revista: Vestn Oftalmol Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Transportadores de Cassetes de Ligação de ATP / Degeneração Macular Limite: Humans Idioma: Ru Revista: Vestn Oftalmol Ano de publicação: 2019 Tipo de documento: Article
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