JI
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| Actin assembly requirements of the formin Fus1 to build the fusion focus | Journal of cell science |  | 2022 | 36 | 0 | ||
| Taurine treatment of retinal degeneration and cardiomyopathy in a consanguineous family with SLC6A6 taurine transporter deficiency | Human Molecular Genetics | | 2020 | 306 | 1 | ||
| Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay | Genetics in Medicine |  | 2018 | 486 | 189 |
