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Identification of the gene for Nance-Horan syndrome (NHS)
Background: The disease intervals for Nance-Horan syndrome (NHS [MIM 302350]) and X linked congenital cataract (CXN) overlap on Xp22. Objective: To identify the gene or genes responsible for these diseases. Methods: Families with NHS were ascertained. The refined locus for CXN was used to focus the...
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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: |
BMJ Group
2004
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1735593/ https://ncbi.nlm.nih.gov/pubmed/15466011 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.022517 |
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