valine has been researched along with Anhidrotic Ectodermal Dysplasia 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 | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cheng, K; Li, W; Liu, S; Luo, L; Ring, BZ; Su, L; Tang, Z; Wang, J; Wang, M; Xu, J; Xue, W; Yang, Y; Zhu, P | 1 |
1 other study(ies) available for valine and Anhidrotic Ectodermal Dysplasia
Article | Year |
---|---|
Novel EDA p.Ile260Ser mutation linked to non-syndromic hypodontia.
Topics: Adolescent; Anodontia; Conserved Sequence; Cuspid; Ectodermal Dysplasia; Ectodysplasins; Exons; Female; Guanine; Humans; Incisor; Isoleucine; Leucine; Male; MSX1 Transcription Factor; Mutation, Missense; PAX9 Transcription Factor; Pedigree; Phenotype; Sequence Homology, Amino Acid; Serine; Structural Homology, Protein; Thymine; Tumor Necrosis Factors; Valine | 2013 |