PTPN11 gene mutation and severe neonatal hypertrophic cardiomyopathy: What is the link?

Keyphrases

• Hypertrophic Cardiomyopathy 100%
• Gene mutation 100%
• PTPN11 Gene 100%
• Noonan Syndrome 75%
• Clinical Features 25%
• Site-directed mutation 25%
• Autosomal Dominant Disorder 25%
• Rapidly Progressive 25%
• Specific mutation 25%
• Multiple Lentigines 25%
• LEOPARD Syndrome 25%
• Dysmorphic Features 25%
• Congenital Heart Defects 25%

Biochemistry, Genetics and Molecular Biology

• Gene Mutation 100%
• PTPN11 100%
• Autosomal Dominant Inheritance 25%