transferrin has been researched along with Neurodevelopmental Disorders in 1 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Al-Gazali, L; Al-Jasmi, F; Antonarakis, SE; Arnold, SJ; Bakey, Z; El-Shanti, H; Eng, CM; Hamamy, H; He, W; Helmstädter, M; Hertecant, J; Hunter, JV; Kambouris, M; Karami Madani, G; Karimiani, EG; Liu, P; Lunke, S; Makrythanasis, P; Maroofian, R; Najafi, M; Petersen, A; Rad, A; Rajab, A; Rehman, AU; Richmond, C; Santoni, FA; Schmidts, M; Stark, Z; Tokita, MJ; Vetrini, F; Walkiewicz, M; Wu, K; Xia, F; Yang, Y | 1 |
1 other study(ies) available for transferrin and Neurodevelopmental Disorders
| Article | Year |
|---|---|
Biallelic loss of function variants in PPP1R21 cause a neurodevelopmental syndrome with impaired endocytic function.
Topics: Adult; Alleles; Child; Child, Preschool; Endocytosis; Endosomes; Female; Fibroblasts; Homozygote; Humans; Infant; Infant, Newborn; Loss of Function Mutation; Male; Myelin Sheath; Neurodevelopmental Disorders; Pedigree; Phosphoprotein Phosphatases; Syndrome; Transferrin | 2019 |