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12-08-2006, 12:10 AM
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Mutation Responsible For Noonan Syndrome Uncovered By Study
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 1000-2500 live births. NS is characterized by short stature facial abnormalities and learning disabilities as well as heart problems and predisposition to leukemia. [click link for aaaa article]Linkleri Üyelerimiz Görebilir. UslanmaM Üyeliği İçin Tıklayın |
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