Carnitine palmitoyltransferase type 2 deficiency: novel mutation in a Native South American family with whole-body muscle magnetic resonance imaging findings: two case reports. https://t.co/HUZcM1tH5g #casereports #jmedicalcasereports https://t.co/HGcAb1DA
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2,891 followers
Carnitine palmitoyltransferase type 2 deficiency: novel mutation in a Native South American family with whole-body muscle magnetic resonance imaging findings: two case reports https://t.co/HUZcM1LhWO #casereports #jmedicalcasereports https://t.co/FgK1vT5W
2,891 followers
Carnitine palmitoyltransferase type 2 deficiency: novel mutation in a Native South American family with whole-body muscle magnetic resonance imaging findings: two case reports https://t.co/HUZcM1LhWO #casereport #jmedicalcasereports https://t.co/5AoLr8Nl1B