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Summary Anatomy Item Literature (8704) Expression Attributions Wiki
XB-ANAT-506

Papers associated with embryonic structure (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.            

Mutations in PYCR1 cause cutis laxa with progeroid features., Reversade B., Nat Genet. September 1, 2009; 41 (9): 1016-21.        

p38 MAP kinase regulates the expression of XMyf5 and affects distinct myogenic programs during Xenopus development., Keren A., Dev Biol. December 1, 2005; 288 (1): 73-86.              

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