Mundlos, S. Research Group Development & Disease (Head: Stefan Mundlos), Max Planck Institute for Molecular Genetics, Max Planck Society; Institute for Medical and Human Genetics Charité, Universitätsmedizin Berlin;
http://www.ncbi.nlm.nih.gov/pubmed/25824905 (beliebiger Volltext)
Sukalo.pdf (Verlagsversion), 373KB
Sukalo, M., Tilsen, F., Kayserili, H., Muller, D., Tuysuz, B., Ruddy, D. M., et al. (2015). DOCK6 mutations are responsible for a distinct autosomal-recessive variant of Adams-Oliver syndrome associated with brain and eye anomalies. Human Mutations, 36(6), 593-598. doi:10.1002/humu.22795.