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The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes
Aims: Multiple genetic causes of congenital cataract have been identified, both as a component of syndromes and in families that present with isolated congenital cataract. Linkage analysis was used to map the genetic locus in a six generation Australian family presenting with total congenital catara...
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| 主要な著者: | , , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Copyright 2005 British Journal of Ophthalmology
2005
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| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1772710/ https://ncbi.nlm.nih.gov/pubmed/15965161 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bjo.2004.058495 |
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