https://ogma.newcastle.edu.au/vital/access/ /manager/Index en-au 5 Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:10874 Sat 24 Mar 2018 08:14:31 AEDT ]]> ALG1-CDG: clinical and molecular characterization of 39 unreported patients https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:28748 Sat 24 Mar 2018 07:37:35 AEDT ]]>