(Q45990056)
Statements
1 reference
Unique haplotype in exon 3 of cone opsin mRNA affects splicing of its precursor, leading to congenital color vision defect. (English)
1 reference
Hisao Ueyama
1 reference
Sanae Muraki-Oda
1 reference
Shinichi Yamade
1 reference
Shoko Tanabe
1 reference
Takahiro Yamashita
1 reference
Yoshinori Shichida
1 reference
Hisakazu Ogita
1 reference
23 June 2012
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424
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1
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152-157
1 reference