Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly
Article in American Journal of Human Genetics (January 2023)
The most recent citing publications are shown below. View all 7 publications that cite this research output on Dimensions.
Novel Homozygous TTI2 Variant Causing Autosomal Recessive Syndromic Intellectual Disability and Primary Microcephaly from Pakistan: A Case Report (Exome Report)
Article in Case Reports in Genetics (August 2022)
Systems genetics in the rat HXB/BXH family identifies Tti2 as a pleiotropic quantitative trait gene for adult hippocampal neurogenesis and serum glucose
Article in PLOS Genetics (April 2022)