A novel mechanism for variable phenotypic expressivity in Mendelian diseases uncovered by an AU-rich element (ARE)-creating mutation

Overview of attention for article published in Genome Biology, July 2017

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RT @alkuraya: Our latest paper! A novel mechanism for variable phenotypic expressivity in Mendelian diseases https://t.co/tZCq0N0K5a

RT @alkuraya: آخر أوراقنا البحثية: اكتشاف كيفية جديدة لحدوث التغاير المظهري للأمراض الوراثية https://t.co/tZCq0N0K5a

RT @alkuraya: آخر أوراقنا البحثية: اكتشاف كيفية جديدة لحدوث التغاير المظهري للأمراض الوراثية https://t.co/tZCq0N0K5a

RT @alkuraya: Our latest paper! A novel mechanism for variable phenotypic expressivity in Mendelian diseases https://t.co/tZCq0N0K5a

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