Ropers, H. H. Emeritus Group of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;
http://www.ncbi.nlm.nih.gov/pubmed/30450701 (beliebiger Volltext)
Kazeminasab.pdf (Verlagsversion), 5MB
Kazeminasab, S., Taskiran, I., Fattahi, Z., Bazazzadegan, N., Hosseini, M., Rahimi, M., et al. (2018). CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability. Am J Med Genet B Neuropsychiatr Genet, 177(8), 691-699. doi:10.1002/ajmg.b.32648.