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APA Citation
Schönewolf‐Greulich, B., Tejada, M., Stephens, K., Hadzsiev, K., Gauthier, J., Brøndum‐Nielsen, K., Pfundt, R., Ravn, K., Maortua, H., Gener, B., Martínez‐Bouzas, C., Piton, A., Rouleau, G., Clayton‐Smith, J., Kleefstra, T., Bisgaard, A., & Tümer, Z. (2016). the MECP2 variant c.925C>T (p.Arg309Trp) causes intellectual disability in both males and females without classic features of Rett syndrome. Clinical genetics, 89(6), 733–738. http://access.bl.uk/ark:/81055/vdc_100032467328.0x000047