Myogenesis defects in a patient-derived iPSC model of hereditary GNE myopathy
R. Schmitt(Institute for Musculoskeletal Health), Jason D. Doles(Universitat Pompeu Fabra), Teerin Liewluck(Mayo Clinic in Arizona), Dong Seong Cho(Mayo Clinic in Arizona), Zhiyv Niu(Mayo Clinic), Douglas Y. Smith(Mayo Clinic in Florida), Zachary T. Resch(Mayo Clinic in Arizona), Margherita Milone(Ospedale Policlinico San Martino), Lindsey A. Kirkeby(Mayo Clinic in Arizona)
Cited by 0
Related Papers
Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders
|New England Journal of Medicine|2013|2k
Molecular diagnostic experience of whole-exome sequencing in adult patients
|Genetics in Medicine|2015|246
Nuclear transformation of Volvox carteri.
|Proceedings of the National Academy of Sciences|1994|168
Neurologic autoimmunity and immune checkpoint inhibitors
|Neurology|2020|158