Rabi Tawil

New findings show abnormally activated parts of a gene called DUX4 may underlie FSH dystrophy

posted on August 27, 2009 - 11:45am
An MDA-supported team of scientists in the United States and the Netherlands has uncovered new leads about the origins of facioscapulohumeral muscular dystrophy (FSHD), a disease whose biochemical underpinnings have proved elusive to scientists despite years of investigation.

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