Complete androgen insensitivity syndrome caused by the R855H mutation in the androgen receptor gene

Keyphrases

• Androgen Receptor Gene 100%
• Androgen Receptor 100%
• Androgen Insensitivity Syndrome 100%
• Receptor-interacting Protein Kinase 1 (RIPK1) 40%
• Protein Molecules 40%
• 46,XY 40%
• Biological Activity 20%
• Guanine 20%
• Codon 20%
• Mutational Analysis 20%
• Phenotypic Expression 20%
• Arginine 20%
• Aunts 20%
• Exon 7 20%
• Amino Acid Sequence 20%
• Genetic Heterogeneity 20%
• Exon 2 20%
• Testicle 20%
• 5-year-old 20%
• XY Karyotype 20%
• Reaction Conditions 20%
• Bilateral Hernia 20%
• Androgen Receptor mutation 20%
• Variable Phenotypic Expression 20%
• Histidine 20%
• Genetic Determinants 20%
• Activation Factor 20%
• Functional Domain 20%
• 46,XX 20%
• Coding Sequence 20%
• Female Phenotype 20%

Biochemistry, Genetics and Molecular Biology

• Receptor Gene 100%
• Androgen Receptor 100%
• Exon 18%
• Protein 18%
• Genetics 9%
• Adenine 9%
• Codon 9%
• Peptide Sequence 9%
• Genetic Heterogeneity 9%
• Biological Activity 9%
• Karyotype 46,XY 9%
• Guanine 9%
• Arginine 9%
• Histidine 9%

Veterinary Science and Veterinary Medicine

• Androgen 100%
• Androgen Receptor 100%
• Hernia 9%