Abstract
Additional file 2. Table S1. Study cohort, disease-related genes, sequencing and variant metrics.
- Title
- Additional file 2 of Shared burden of ultra-rare genetic variants across a spectrum of motor neuron diseases
- Creators
- Gang Wu - St. Jude Children's Research HospitalWenan Chen - St. Jude Children's Research HospitalJoanne Wuu - University of MiamiAngita Jain - WinnMedJason Myers - St. Jude Children's Research HospitalIsabell Cordts - WinnMedEvadnie Rampersaud - St. Jude Children's Research HospitalJeannine M. Heckmann - University of Cape TownMelissa Nel - University of Cape TownVolkan Granit - University of MiamiJeffrey Statland - University of KansasAndrea Swenson - University of IowaJohn Ravits - University of California San DiegoCorey T. McMillan - California University of PennsylvaniaLauren Elman - University of PennsylvaniaJames Caress - Wake Forest UniversityTed M. BurnsErik P. Pioro - University of British ColumbiaJaya Trivedi - The University of Texas Southwestern Medical CenterJonathan Katz - California Pacific Medical CenterCarlayne Jackson - The University of Texas Health Science Center at San AntonioSamuel Maiser - University of Minnesota SystemDavid Walk - University of Minnesota SystemYuen So - Stanford UniversityJacob L. McCauley - University of MiamiMatthew C. Baker - WinnMedJ. Paul Taylor - St. Jude Children's Research HospitalStephan Zuchner - University of MiamiRosa Rademakers - University of AntwerpMarka van Blitterswijk - WinnMedMichael Benatar - University of Miami
- Publisher
- figshare
- Academic Unit
- Leadership Department; Miller School of Medicine; UMMG Department of Neurology; UMMG Dept of Human Genetics (Dr. John T. Macdonald Foundation); UMMG Dept of Neurology - Neuromuscular Disorders Div; John P. Hussman Institute for Human Genomics
- Language
- English
- Resource Type
- Dataset
- Record Identifier
- 991032856229502976