adenine has been researched along with Familial Hypophosphatemic Rickets in 1 studies
Familial Hypophosphatemic Rickets: A hereditary disorder characterized by HYPOPHOSPHATEMIA; RICKETS; OSTEOMALACIA; renal defects in phosphate reabsorption and vitamin D metabolism; and growth retardation. Autosomal and X-linked dominant and recessive variants have been reported.
| 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 | 0 (0.00) | 24.3611 |
| 2020's | 1 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alhamoudi, KM | 1 |
| Alghamdi, B | 1 |
| Alswailem, M | 1 |
| Nasir, A | 1 |
| Aljomaiah, A | 1 |
| Al-Hindi, H | 1 |
| Alzahrani, AS | 1 |
1 other study available for adenine and Familial Hypophosphatemic Rickets
| Article | Year |
|---|---|
A Unique Mechanism of a Novel Synonymous PHEX Variant Causing X-Linked Hypophosphatemia.
Topics: Adenine; Amino Acids; Codon, Terminator; Cytosine; DNA, Complementary; Familial Hypophosphatemic Ric | 2022 |