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首页> 外文期刊>The National medical journal of India >Association of presenile cataract with galactose-1-phosphate uridyl transferase gene mutations
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Association of presenile cataract with galactose-1-phosphate uridyl transferase gene mutations

机译:高分子白内障与半乳糖-1-磷酸尿苷转移酶基因突变的关联

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摘要

Background. Presenile cataract is commonly idiopathic in origin. However, patients with presenile cataract could have an underlying genetic abnormality of galactose metabolism. We studied the association, if any, between idiopathic presenile cataract and galactose-l-phosphate uridyl transferase (GALT) gene mutation.
机译:出身背景老年前期白内障通常起源于特发性。然而,老年前期白内障患者可能存在半乳糖代谢的潜在遗传异常。我们研究了特发性老年前期白内障与半乳糖-l-磷酸尿苷转移酶(GALT)基因突变之间的关联。

著录项

  • 来源
  • 作者单位

    Sri Aurobindo Med Coll &

    PG Inst Dept Ophthalmol Indore Ujjain Highway Indore Madhya Pradesh;

    Sri Aurobindo Med Coll &

    PG Inst Cent Res Lab Indore Ujjain Highway Indore Madhya Pradesh India;

    Sri Aurobindo Med Coll &

    PG Inst Dept Ophthalmol Indore Ujjain Highway Indore Madhya Pradesh;

    Sri Aurobindo Med Coll &

    PG Inst Dept Ophthalmol Indore Ujjain Highway Indore Madhya Pradesh;

    Sri Aurobindo Med Coll &

    PG Inst Cent Res Lab Indore Ujjain Highway Indore Madhya Pradesh India;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医药、卫生;
  • 关键词

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