Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes

Author: Martinelli Simone   Torreri Paola   Tinti Michele   Stella Lorenzo   Bocchinfuso Gianfranco   Flex Elisabetta   Grottesi Alessandro   Ceccarini Marina   Palleschi Antonio   Cesareni Gianni   Castagnoli Luisa   Petrucci Tamara C.   Gelb Bruce D.   Tartaglia Marco  

Publisher: Oxford University Press

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.17, Iss.13, 2008-07, pp. : 2018-2029

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