The 2p21 deletion syndrome: Characterization of the transcription content

Keyphrases

• Expression Pattern 100%
• Splice Variant 100%
• Deletion Syndrome 100%
• Mitochondria 50%
• First Exons 50%
• Genotype-phenotype Correlation 50%
• Upstream Open Reading Frame (uORF) 50%
• Developmental Delay 50%
• Homozygous Deletion 50%
• Magnesium 50%
• Reducing Activity 50%
• Enzymatic Complex 50%
• Hypotonia 50%
• Cystinuria 50%
• Facial Dysmorphism 50%
• Neonatal Seizures 50%
• Haploinsufficiency 50%
• Gene Symbols 50%
• PREPL 50%
• SLC3A1 50%
• PPM1B 50%
• Respiratory Chain 50%
• Protein Phosphatase 1B 50%
• Small Deletion 50%

Biochemistry, Genetics and Molecular Biology

• Transcription 100%
• Mitochondrion 50%
• Exon 50%
• Isoform 50%
• Open Reading Frame 50%
• Genotype Phenotype Correlation 50%
• Electron Transport Chain 50%
• Dominant Inheritance 50%
• Haploinsufficiency 50%
• Phosphoprotein Phosphatase 50%
• SLC3A1 50%