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Exon 3 genotypes of OPN1LW/OPN1MW associated with X-linked congenital cone dysfunction
- Kohl, S (author)
- Baumann, B (author)
- Hamel, C (author)
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- Gustavsson, P (author)
- Rosenberg, T (author)
- Plomp, A (author)
- Leroy, B (author)
- Verheij, JBGM (author)
- Wissinger, B (author)
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- 2013
- 2013
- English.
- In: INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. - 0146-0404. ; 54:15
- Conference paper (other academic/artistic)
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- vet (subject category)
- kon (subject category)
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- Kohl, S
- Baumann, B
- Hamel, C
- Gustavsson, P
- Rosenberg, T
- Plomp, A
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- Leroy, B
- Verheij, JBGM
- Wissinger, B
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- INVESTIGATIVE OP ...
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- Karolinska Institutet
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