leucine has been researched along with Anhidrotic Ectodermal Dysplasia in 2 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 | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Anzai, M; Aoki, Y; Endo, W; Haginoya, K; Inui, T; Kikuchi, A; Kure, S; Miyabayashi, T; Nagai, K; Niihori, T; Okubo, Y; Sato, R; Suzuki-Muromoto, S; Takezawa, Y; Togashi, N; Yamamura-Suzuki, S | 1 |
| 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 |
2 other study(ies) available for leucine and Anhidrotic Ectodermal Dysplasia
| Article | Year |
|---|---|
Leucine-485 deletion variant of BRAF may exhibit the severe end of the clinical spectrum of CFC syndrome.
Topics: Amino Acid Sequence; Child, Preschool; Ectodermal Dysplasia; Facies; Failure to Thrive; Heart Defects, Congenital; Humans; Leucine; Male; Proto-Oncogene Proteins B-raf; Sequence Deletion; Severity of Illness Index | 2019 |
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 |