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Paper Details

Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis.
Neuromuscul Disord
1
2023
Author NameAffiliation
Nigel G LaingCentre for Medical Research University of Western Australia, Harry Perkins Institute of Medical Research, QEII Medical Centre
Karin S KassahnAdelaide Medical School, The University of Adelaide
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Datasets

Release 1.2