Deletion/insertion mutation that causes biotinidase deficiency may result from the formation of a quasipalindromic structure

Keyphrases

• Insertion mutation 100%
• Biotinidase Deficiency 100%
• Biotinidase 100%
• Biotin 50%
• In Vitro Study 50%
• Exon 50%
• Eukaryotes 50%
• Polymerase 50%
• Biocytin 50%
• Dissociation 50%
• DNA Replication 50%
• DNA Polymerase 50%
• Possible Causes 50%
• Vitamins 50%
• Frameshift 50%
• Truncated Protein 50%
• Premature Termination 50%
• Proteolytic Degradation 50%
• Hairpin Loop 50%
• Biotin Carboxylase 50%
• Palindromic Structure 50%

Biochemistry, Genetics and Molecular Biology

• Indel 100%
• Biotinidase 100%
• DNA Template 50%
• Biotin 50%
• Polymerase 25%
• In Vitro Study 25%
• Exon 25%
• Eukaryote 25%
• DNA Synthesis 25%
• DNA Polymerase 25%