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APA Citation

    Di Donato, N., Neuhann, T., Kahlert, A., Klink, B., Hackmann, K., Neuhann, I., Novotna, B., Schallner, J., Krause, C., Glass, I. A., Parnell, S. E., Benet-Pages, A., Nissen, A. M., Berger, W., Altmüller, J., Thiele, H., Weber, B. H. F., Schrock, E., Dobyns, W. B., Bier, A., & Rump, A. (2016). mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt. Journal of medical genetics, 53(6), 419–425. http://access.bl.uk/ark:/81055/vdc_100135181785.0x000041
  
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