@article{oai:tsukuba.repo.nii.ac.jp:00037020,
 author = {野口, 惠美子 and Song, Hao and Makino, Yuka and Noguchi, Emiko and Arinami, Tadao},
 issue = {2},
 journal = {Clinical Case Reports},
 month = {Feb},
 note = {The FOXP protein family (FOXP1-4) is a group of transcription factors that play important roles in embryological, immunological, hematological, and speech and language development. Here, we report FOXP1 de novo mutation and severe speech delay in an individual belonging to a non-Caucasian population.},
 pages = {110--113},
 title = {A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment},
 volume = {3},
 year = {2015}
}