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Human Mutation|August 23, 2020
Renal dysfunction, rod-cone dystrophy, and sensorineural hearing loss caused by a mutation in RRM2BLisa Roberts, Stephanie Julius, Shrinav Dawlat, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 15, 2010
Mutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndromeBrian P Kelley, Fransiska Malfait, Luisa Bonafe, et al.American Journal of Respiratory and Critical Care Medicine|June 8, 2018
Drug-Penetration Gradients Associated with Acquired Drug Resistance in Patients with TuberculosisKeertan Dheda, Laura Lenders, Gesham Magombedze, et al.American Journal of Respiratory and Critical Care Medicine|January 30, 2019
Spatial Network Mapping of Pulmonary Multidrug-Resistant Tuberculosis Cavities Using RNA SequencingKeertan Dheda, Laura Lenders, Shashikant Srivastava, et al.International Journal of Cardiology|February 19, 2021
Rationale and design of the African Cardiomyopathy and Myocarditis Registry Program: The IMHOTEP studySarah M Kraus, Gasnat Shaboodien, Veronica Francis, et al.Pageof 7