¹Järvelä, I., Määttä, T., Acharya, A. et al. Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland. Hum Genet 140, 1011–1029 (2021). https://doi.org/10.1007/s00439-021-02268-1

 2,264 total views,  19 views today