glycine has been researched along with Congenital Erythropoietic Porphyria in 1 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Congenital erythropoietic porphyria (CEP) is a rare autosomal recessive disease caused by the deficient activity of the heme biosynthetic enzyme, uroporphyrinogen III synthase (URO-synthase), and the accumulation of the nonphysiologic and phototoxic porphyrin I isomers." | 1.33 | Two brothers with mild congenital erythropoietic porphyria due to a novel genotype. ( Astrin, KH; Berry, AA; Desnick, RJ; Lim, HW; Lucky, AW; Shabbeer, J, 2005) |
| 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 |
|---|---|
| Berry, AA | 1 |
| Desnick, RJ | 1 |
| Astrin, KH | 1 |
| Shabbeer, J | 1 |
| Lucky, AW | 1 |
| Lim, HW | 1 |
1 other study available for glycine and Congenital Erythropoietic Porphyria
| Article | Year |
|---|---|
Two brothers with mild congenital erythropoietic porphyria due to a novel genotype.
Topics: Adolescent; Alanine; Child, Preschool; Exons; Genetic Counseling; Genotype; Glycine; Humans; Male; M | 2005 |