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OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium. [electronic resource] by
- Vincent, Ajoy
- Forster, Nicole
- Maynes, Jason T
- Paton, Tara A
- Billingsley, Gail
- Roslin, Nicole M
- Ali, Arfan
- Sutherland, Joanne
- Wright, Tom
- Westall, Carol A
- Paterson, Andrew D
- Marshall, Christian R
- Héon, Elise
Producer: 20150709
In:
Journal of medical genetics vol. 51
Availability: No items available.
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