Not Signed In - Study Uncovers Mutation Responsible For Noonan Syndrome
Tue, 05 Dec 2006 04:00 AM EST
... Scientists have discovered that mutations in a gene known as SOS1 account for many cases of Noonan syndrome (NS), a common childhood genetic disorder which occurs in one in 1,000-2,500 live births. NS is characterized by short stature, facial abnormalities and learning disabilities, as well as heart problems and predisposition to leukemia. ...
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