Characterization of frequent deletions causing steroid 21-hydroxylase deficiency

Biochemistry, Genetics and Molecular Biology

• 21-Hydroxylase 100%
• Gene Conversion 100%
• Chromosome 15 80%
• EcoRI 60%
• Pseudogene 40%
• C4A 40%
• Allele 20%
• Oxygenase 20%
• Oligonucleotide Probe 20%
• Restriction Enzyme 20%
• Isoprenaline 20%

Keyphrases

• 21-Hydroxylase Deficiency (21OHD) 100%
• Gene Conversion 100%
• TaqI 80%
• EcoRI 60%
• Pseudogene 40%
• Oligonucleotide Probes 20%
• Multifunctional Protein 20%
• Restriction Enzyme 20%
• Deleterious mutations 20%
• 21-hydroxylase 20%
• P21 Gene 20%