Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes
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| Description | scientific article |
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author: Bruce D. Gelb Gianni Cesareni Alessandro Grottesi Luisa Castagnoli Marco Tartaglia Paola Torreri Gianfranco Bocchinfuso Lorenzo Stella |
| Publication date | March 27, 2008 |
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