Sığırcı, AhmetAlkan, AlpayKutlu, RamazanGülcan, Hande2017-06-232017-06-232005Sığırcı, A. Alkan, A. Kutlu, R. Gülcan, H. (2005). Multivoxel magnetic resonance spectroscopy in a rhizomelic chondrodysplasia punctata case. J Child Neurol. 20- (8); 698-701.https://hdl.handle.net/11616/7155We screened 29 children with autism for mutation in the human secretin gene using single-strand conformation polymorphism. No mutation was detected in exon 2, 3, or 4. Polymerase chain reaction and DNA sequence of 5´ variable number of tandem repeats showed two polymorphisms with deletion or duplication of a repeat unit that failed to show any gene expression with transient transfection assay. We did not find evidence of a relationship between human secretin gene mutation and autism.eninfo:eu-repo/semantics/openAccessArticle208698701