leucine has been researched along with Genetic Diseases, X-Chromosome Linked 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 | 1 (50.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Hyun, HK; Kim, JW; Ko, J; Lee, KE; Lee, SH; Shin, TJ | 1 |
Burke, DW; Butler, MG; Campbell, CA; Chang, EH; Forrester, S; Hoppe, JE; Schneider, MC; Smith, LL; Smith, RJ; Vore, AP | 1 |
2 other study(ies) available for leucine and Genetic Diseases, X-Chromosome Linked
Article | Year |
---|---|
Oligodontia and curly hair occur with ectodysplasin-a mutations.
Topics: Anodontia; Arginine; Child; Child, Preschool; Codon; Conserved Sequence; Ectodysplasins; Exome; Gene Frequency; Genetic Diseases, X-Linked; Genetic Variation; Guanine; Hair; Humans; Leucine; Male; Mutation, Missense; Pedigree; Phenylalanine; Signal Transduction; Thymine; Valine | 2014 |
Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafness.
Topics: Chromosome Deletion; Chromosome Segregation; Deafness; Female; Genetic Diseases, X-Linked; Humans; Leucine; Male; Mutation, Missense; Pedigree; POU Domain Factors; Sensory Thresholds; Serine; Temporal Bone; Tomography, X-Ray Computed | 2005 |