[Familial high myopia--challenge of modern genetics]
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Updated: Sep 23, 2026

A Phenotyping Regimen for Genetically Modified Mice Used to Study Genes Implicated in Human Diseases of Aging
Published on: July 14, 2016
Joanna Adamiec1, Maria Hanna Nizankowska
1Katedry i Kliniki Okulistyki Akademii Medycznej we Wrocławiu.
Abstract:
In this paper has been accomplished an estimation of contemporary achievement in molecular researches domain's of pathology in familial high myopia. Clinical observations of monozygotic and dizygotic twins groups and also among family members with this type of myopia disclosing in following generations show, that it has inborn character. Nowadays, it has been identified three gen locci connected with heritage of this illness unit: 18p11.31, 12q21-31, 7q36. Above incontestable achievements do not interpret mechanism uprising this disease. Problem is still, to define the products planned by exchanged area of DNA, conditioning progress of high familial myopia.
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