Bujakowska, K. M., Zhang, Q., Siemiatkowska, A. M., Liu, Q., Place, E., Falk, M. J., . . . Pierce, E. A. (2015). Mutations in IFT172 cause isolated retinal degeneration and Bardet–Biedl syndrome. Hum Mol Genet.
Style de citation ChicagoBujakowska, Kinga M., et al. "Mutations in IFT172 Cause Isolated Retinal Degeneration and Bardet–Biedl Syndrome." Hum Mol Genet 2015.
Style de citation MLABujakowska, Kinga M., et al. "Mutations in IFT172 Cause Isolated Retinal Degeneration and Bardet–Biedl Syndrome." Hum Mol Genet 2015.
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