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XB-ANAT-226
Papers associated with optic vesicle (and pycr1)
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A truncated form of rod photoreceptor PDE6 β-subunit causes autosomal dominant congenital stationary night blindness by interfering with the inhibitory activity of the γ-subunit., Manes G., PLoS One. January 1, 2014; 9 (4): e95768. |
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Mutations in PYCR1 cause cutis laxa with progeroid features., Reversade B., Nat Genet. September 1, 2009; 41 (9): 1016-21. |
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