Scientists Make Groundbreaking Discovery Of Mutation Causing Genetic Disorder In Humans - Scientists at A*STAR's Institute of Medical Biology, in collaboration with doctors and scientists in Jordan, Turkey, Switzerland and USA, have identified the genetic cause of a birth defect known as Hamamy syndrome. Their groundbreaking findings were published in the prestigious journal Nature Genetics and lend new insights into common ailments such as heart disease, osteoporosis, blood disorders and possibly sterility. Reference: “Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1,” C. Bonnard et al, Nature Genetics 2012; DOI: 10.1038/ng.2259
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ChemSpy.com is owned and operated by science journalist David Bradley. Additional chemistry news updates are posted by chemist Robert Slinn CChem MRSC MPhil with the tag: Slinn Pickings.





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