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

Source:http://linkedlifedata.com/resource/pubmed/id/18372317

Hum. Mol. Genet. 2008 Jul 1 17 13 2018-29

Download in:

View as

Triples

General Info

PMID
18372317