Recessive PYROXD1 mutations cause adult-onset limb-girdle-type muscular dystrophy. #amchelsinki #tutkimus https://t.co/vWgpwjqL07
RT @MetaStem_Center: New findings on adult-onset myopathy from our CoE by Sainio et al @HTyynismaa lab out in Journal of #neurology. Recess…
RT @MetaStem_Center: New findings on adult-onset myopathy from our CoE by Sainio et al @HTyynismaa lab out in Journal of #neurology. Recess…
RT @MetaStem_Center: New findings on adult-onset myopathy from our CoE by Sainio et al @HTyynismaa lab out in Journal of #neurology. Recess…
RT @MetaStem_Center: New findings on adult-onset myopathy from our CoE by Sainio et al @HTyynismaa lab out in Journal of #neurology. Recess…
RT @MetaStem_Center: New findings on adult-onset myopathy from our CoE by Sainio et al @HTyynismaa lab out in Journal of #neurology. Recess…
RT @HTyynismaa: PYROXD1 oxidoreductase mutations in adult-onset myopathy - new paper from our pHealth @Aka_ohjelmat @helsinkiuni @amchelsin…
RT @MetaStem_Center: New findings on adult-onset myopathy from our CoE by Sainio et al @HTyynismaa lab out in Journal of #neurology. Recess…
RT @MetaStem_Center: New findings on adult-onset myopathy from our CoE by Sainio et al @HTyynismaa lab out in Journal of #neurology. Recessive variants in PYROXD1 patients with limb-girdle-type muscular dystrophy. https://t.co/MZorNM1ASl @helsinkiuni @amch
RT @MetaStem_Center: New findings on adult-onset myopathy from our CoE by Sainio et al @HTyynismaa lab out in Journal of #neurology. Recess…
New findings on adult-onset myopathy from our CoE by Sainio et al @HTyynismaa lab out in Journal of #neurology. Recessive variants in PYROXD1 patients with limb-girdle-type muscular dystrophy. https://t.co/GpfhIrIXn5 @helsinkiuni @amchelsinki @MolNeuroProg
RT @HTyynismaa: PYROXD1 oxidoreductase mutations in adult-onset myopathy - new paper from our pHealth @Aka_ohjelmat @helsinkiuni @amchelsin…
RT @HTyynismaa: PYROXD1 oxidoreductase mutations in adult-onset myopathy - new paper from our pHealth @Aka_ohjelmat @helsinkiuni @amchelsin…
RT @HTyynismaa: PYROXD1 oxidoreductase mutations in adult-onset myopathy - new paper from our pHealth @Aka_ohjelmat @helsinkiuni @amchelsin…
RT @HTyynismaa: PYROXD1 oxidoreductase mutations in adult-onset myopathy - new paper from our pHealth @Aka_ohjelmat @helsinkiuni @amchelsin…
RT @HTyynismaa: PYROXD1 oxidoreductase mutations in adult-onset myopathy - new paper from our pHealth @Aka_ohjelmat @helsinkiuni @amchelsin…
RT @HTyynismaa: PYROXD1 oxidoreductase mutations in adult-onset myopathy - new paper from our pHealth @Aka_ohjelmat @helsinkiuni @amchelsin…
PYROXD1 oxidoreductase mutations in adult-onset myopathy - new paper from our pHealth @Aka_ohjelmat @helsinkiuni @amchelsinki https://t.co/3EnIKiGiip