## Abstract Germ line gainβofβfunction mutations in several members of the RAS/ERK pathway, including __PTPN11__, __KRAS__, and __RAF1,__ cause the autosomal dominant genetic disorder Noonan Syndrome (NS). NS patients are at increased risk of leukemia/myeloproliferative disease and possibly some so
Are ECG abnormalities in Noonan syndrome characteristic for the syndrome?
β Scribed by R. Raaijmakers; C. Noordam; J. A. Noonan; E. A. Croonen; C. J. A. M. van der Burgt; J. M. T. Draaisma
- Publisher
- Springer
- Year
- 2008
- Tongue
- English
- Weight
- 131 KB
- Volume
- 167
- Category
- Article
- ISSN
- 0340-6997
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