Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis
Titel:
Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis
Auteur:
Ghaoui, Roula Ha, Thuong T. Kerkhof, Jennifer McConkey, Haley Gao, Song Babic, Milena King, Rob Ravenscroft, Gianina Koszyca, Barbara Otto, Sophia Laing, Nigel G. Scott, Hamish Sadikovic, Bekim Kassahn, Karin S.