Supplementary information

From the following article

Germline gain-of-function mutations in SOS1 cause Noonan syndrome

Amy E Roberts, Toshiyuki Araki, Kenneth D Swanson, Kate T Montgomery, Taryn A Schiripo, Victoria A Joshi, Li Li, Yosuf Yassin, Alex M Tamburino, Benjamin G Neel & Raju S Kucherlapati

Nature Genetics 39, 70 - 74 (2007)

doi:10.1038/ng1926

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Supplementary Fig. 1

Noonan syndrome–associated SOS1 mutants cause sustained ERK activation.

Supplementary Fig. 2

Noonan syndrome–associated SOS1 mutants enhance endogenous ERK activation.

Supplementary Table 1

Genotype-phenotype correlations in Noonan syndrome

Supplementary Table 2

Primer pairs used for gene amplification.

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