threonine has been researched along with Aldosteronism with Hyperplasia of the Adrenal Cortex 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 |
---|---|
Bilbao, JR; Castaño, L; Pérez de Nanclares, G; Rodríguez-Soriano, J; Vallo, A | 1 |
1 other study(ies) available for threonine and Aldosteronism with Hyperplasia of the Adrenal Cortex
Article | Year |
---|---|
A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain.
Topics: Adolescent; Alanine; Amino Acid Substitution; Anion Transport Proteins; Bartter Syndrome; Base Sequence; Child; Child, Preschool; Chloride Channels; DNA Mutational Analysis; Founder Effect; Genotype; Homozygote; Humans; Infant; Membrane Proteins; Mutation, Missense; Phenotype; Point Mutation; Spain; Threonine | 2005 |