adenine has been researched along with Hermanski-Pudlak Syndrome in 1 studies
Hermanski-Pudlak Syndrome: Syndrome characterized by the triad of oculocutaneous albinism (ALBINISM, OCULOCUTANEOUS); PLATELET STORAGE POOL DEFICIENCY; and lysosomal accumulation of ceroid lipofuscin.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Suzuki, T | 1 |
| Ito, S | 1 |
| Inagaki, K | 1 |
| Suzuki, N | 1 |
| Tomita, Y | 1 |
| Yoshino, M | 1 |
| Hashimoto, T | 1 |
1 other study available for adenine and Hermanski-Pudlak Syndrome
| Article | Year |
|---|---|
Investigation on the IVS5 +5G --> a splice site mutation of HPS1 gene found in Japanese patients with Hermansky-Pudlak syndrome.
Topics: Adenine; Asian People; Child, Preschool; DNA, Recombinant; Guanine; Hermanski-Pudlak Syndrome; Human | 2004 |