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APA Citation
Khan, A. O., Decker, E., Bachmann, N., Bolz, H. J., & Bergmann, C. (2016). c8orf37 is mutated in Bardet-Biedl syndrome and constitutes a locus allelic to non-syndromic retinal dystrophies. Ophthalmic genetics, 37, 290–293. http://access.bl.uk/ark:/81055/vdc_100034566536.0x00002f