Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction

Biochemistry, Genetics and Molecular Biology

• PHOX2B 100%
• Transcription Factor 50%
• Whole Genome Sequencing 50%
• Myosin 50%
• Molecular Motor 50%
• Motor Protein 50%
• Homozygosity 50%
• Breathing 50%
• Respiration Control 50%
• CRISPR/Cas9 50%
• Mutant Mouse Strain 50%
• Exon 50%
• Intracellular Transport 50%

Medicine and Dentistry

• Hypoventilation 100%
• Carbon Dioxide 75%
• Congenital Central Hypoventilation Syndrome 50%
• Exon 25%
• Knock Out 25%
• Pathogenicity 25%
• Medulla 25%
• Clustered Regularly Interspaced Short Palindromic Repeat 25%
• Plethysmography 25%
• Intracellular Transport 25%
• Transcription Factor 25%
• Airway Management 25%
• Cas9 25%
• Motor Protein 25%
• Lung Alveolus Hypoventilation 25%