Mutations in RIT1 cause Noonan syndrome - additional functional evidence and expanding the clinical phenotype

Medicine and Dentistry

• Phenotype 100%
• Noonan Syndrome 100%
• Protein 66%
• Lymphedema 66%
• Mitogen-Activated Protein Kinase 66%
• Patient 33%
• Aptitude 33%
• Organism 33%
• Mutant 33%
• Guanosine Triphosphatase 33%
• Eye Development 33%
• Hygroma 33%
• Guanosine Triphosphatase Activating Protein 33%

Biochemistry, Genetics and Molecular Biology

• Phenotype 100%
• Spectrum 66%
• Protein 66%
• Mitogen-Activated Protein Kinase 66%
• Wild Type 33%
• GTPase-activating Protein 33%
• Missense 33%
• Aptitude 33%
• Zebra Fish 33%
• Organisms 33%
• Mutant 33%
• Eye Development 33%
• GTPase 33%

Immunology and Microbiology

• Phenotype 100%
• Mitogen 66%
• Spectrum 66%
• Aptitude 33%
• Organisms 33%
• Mutant 33%
• Zebra Fish 33%
• Eye Development 33%
• Wild Type 33%