PTPN11 (Shp2) Mutations in LEOPARD Syndrome Have Dominant Negative, Not Activating, Effects
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference42 articles.
1. NOONAN SYNDROME AND RELATED DISORDERS: Genetics and Pathogenesis
2. Grouping of Multiple-Lentigines/LEOPARD and Noonan Syndromes on the PTPN11 Gene
3. PTPN11 mutations in LEOPARD syndrome
4. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
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