Recurrent arginine substitutions in the ACTG2 gene are the primary driver of disease burden and severity in visceral myopathy
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| Description | scientific article published on 19 December 2019 |
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author: Baylor-Hopkins Center for Mendelian Genomics Jennifer E. Posey Michael F. Wangler Ronit Marom Robert Smigiel Zeynep Coban Akdemir James R. Lupski Maciej Bagłaj Bert Callewaert |
| Publication date | December 19, 2019 |
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