Congenital Central Hypoventilation Syndrome (CCHS) and PHOX2B Mutations

Medicine and Dentistry

• Genotype 100%
• Autonomic Nervous System 100%
• Frameshift Mutation 100%
• Congenital Central Hypoventilation Syndrome 100%
• Airway Management 100%
• Development 50%
• Neural Crest 50%
• Transcription Factor 50%
• Human Embryo 50%
• Exon 50%
• Hypercapnia 50%
• Hypoxemia 50%
• Hypoventilation 50%
• K-Complex 50%
• Neuron 50%
• Dependent Personality Disorder 50%
• Rest 50%
• Activities of Daily Living 50%
• Sleep 50%

INIS

• mutations 100%
• congenital diseases 100%
• control 66%
• genotype 66%
• autonomic nervous system 66%
• psychological behavior 33%
• mice 33%
• rodents 33%
• humans 33%
• neurons 33%
• transcription factors 33%
• sleep 33%
• exons 33%
• embryos 33%
• reflexes 33%