Straub, V. W.

Top Publications

Top Publications Authored or Co-Authored by "Straub, V. W."

• RYR1 mutations are a common cause of congenital myopathies with central nuclei

  Annals of Neurology, Volume 68, No. 5, Year 2010, Citations 233
• Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2

  Brain, Volume 137, No. 1, Year 2014, Citations 149
• Mild congenital muscular dystrophy in two patients with an internally deleted laminin α2-chain

  Human Molecular Genetics, Volume 6, No. 5, Year 1997, Citations 138
• Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database

  Journal of Neuromuscular Diseases, Volume 4, No. 4, Year 2017, Citations 116
• Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness

  Genetics in Medicine, Volume 22, No. 9, Year 2020, Citations 99