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APA Citation

    Rad, A., Altunoglu, U., Miller, R., Maroofian, R., James, K. N., Çağlayan, A. O., Najafi, M., Stanley, V., Boustany, R., Yeşil, G., Sahebzamani, A., Ercan-Sencicek, G., Saeidi, K., Wu, K., Bauer, P., Bakey, Z., Gleeson, J. G., Hauser, N., Gunel, M., Kayserili, H., & Schmidts, M. (2019). mAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome). Journal of medical genetics, 56(5), 332–339. http://access.bl.uk/ark:/81055/vdc_100135161177.0x00002f
  
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