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

Title
Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes
Authors
Keywords
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Journal
HUMAN MOLECULAR GENETICS
Volume 17, Issue 13, Pages 2018-2029
Publisher
Oxford University Press (OUP)
Online
2008-03-28
DOI
10.1093/hmg/ddn099

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