leucine has been researched along with Congenital Erythropoietic Porphyria 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 | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
de Verneuil, H; Ged, C; Herrero, C; Lecha, M; Mascaro, JM; Mendez, M; Ozalla, D | 1 |
1 other study(ies) available for leucine and Congenital Erythropoietic Porphyria
Article | Year |
---|---|
Description of a new mutation in hepatoerythropoietic porphyria and prenatal exclusion of a homozygous fetus.
Topics: Amino Acid Substitution; Child, Preschool; Chromosome Aberrations; Codon; Consanguinity; Female; Genes, Recessive; Genetic Carrier Screening; Homozygote; Humans; Leucine; Male; Mutation; Phenylalanine; Porphyria, Erythropoietic; Pregnancy; Prenatal Diagnosis; Uroporphyrinogen Decarboxylase | 2002 |