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

标题
Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume 17, Issue 13, Pages 2018-2029
出版商
Oxford University Press (OUP)
发表日期
2008-03-28
DOI
10.1093/hmg/ddn099

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