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HARVARD Citation
Khan, A. et al. (2016). C8orf37 is mutated in Bardet-Biedl syndrome and constitutes a locus allelic to non-syndromic retinal dystrophies. Ophthalmic genetics. pp. 290-293. [Online].
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Khan, A. et al. (2016). C8orf37 is mutated in Bardet-Biedl syndrome and constitutes a locus allelic to non-syndromic retinal dystrophies. Ophthalmic genetics. pp. 290-293. [Online].