Unique haplotype in exon 3 of cone opsin mRNA affects splicing of its precursor, leading to congenital color vision defect. (Q45990056)
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scientific article published on 23 June 2012
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Unique haplotype in exon 3 of cone opsin mRNA affects splicing of its precursor, leading to congenital color vision defect. |
scientific article published on 23 June 2012 |
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Unique haplotype in exon 3 of cone opsin mRNA affects splicing of its precursor, leading to congenital color vision defect. (English)
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Hisao Ueyama
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Sanae Muraki-Oda
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Shinichi Yamade
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Shoko Tanabe
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Takahiro Yamashita
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Yoshinori Shichida
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Hisakazu Ogita
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23 June 2012
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424
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1
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152-157
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