Secondary NAD<sup>+</sup> deficiency in the inherited defect of glutamine synthetase
Liyan Hu(Gansu Agricultural University), Johannes Häberle(University Children's Hospital Zurich), Tawfeg Ben‐Omran(Qatar Airways (Qatar)), Farrukh A. Chaudhry(University of Oslo), William Todd Penberthy, Noora Shahbeck(Hamad Medical Corporation), Michele Frapolli(University Children's Hospital Zurich), Khalid Ibrahim, Boris Görg(Düsseldorf University Hospital), Martin Stucki(University Children's Hospital Zurich), Dieter Häussinger(Heinrich Heine University Düsseldorf)
Cited by 22
Related Papers
Nusinersen initiated in infants during the presymptomatic stage of spinal muscular atrophy: Interim efficacy and safety results from the Phase 2 NURTURE study
|Neuromuscular Disorders|2019|636
Suggested guidelines for the diagnosis and management of urea cycle disorders
|Orphanet Journal of Rare Diseases|2012|627