Identification of novel homozygous nonsense SLC10A7 variant causing short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis and surgical management of spine
Article in Orphanet Journal of Rare Diseases (November 2023)
The most recent citing publications are shown below. View all 6 publications that cite this research output on Dimensions.
Article in Orphanet Journal of Rare Diseases (November 2023)
Article in Human Genetics (January 2022)
Article in Nature Communications (August 2018)