This study offers important insight into the pathogenic basis of intragenic frameshift deletions in the carboxy-terminal domain of MECP2, which account for some Rett syndrome cases, yet similar ...
A graph-based computational tool for detecting previously invisible genetic mutations has been developed. Researchers at the University of California, Los Angeles (UCLA; USA) and the University of ...
The analysis revealed that about 2 per cent of sperm from men in their early 30s contained disease-causing mutations. That ...
Variations in the properties of arabica coffee, such as in taste, caffeine content and disease resistance, are determined by chromosome mutations, according to a recent study. But are these findings ...
Santhosh Girirajan receives funding from the National Institutes of Health. Genetic inheritance may sound straightforward: One gene causes one trait or a specific illness. When doctors use genetics, ...
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Confirming the effectiveness of targeted therapy for gene mutation that causes hearing loss...Up to ...
A treatment that is effective against hearing loss caused by the 'MPZL2 gene' mutation has been developed. A research team ...
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