Related Experiment Videos
Gene symbol: OTC. Disease: ornithine carbamoyltransferase deficiency
Wuh-Liang Hwu1, Yuan-Te Huang, Yin-Hsu Chien
1Department of Pediatrics and Medical Genetics, National Taiwan University Hospital, Taipei. hwu@ha.mc.ntu.edu.tw
Human Genetics
|September 17, 2003
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Cognitive development in children with Prader-Willi syndrome receiving early growth hormone therapy.
Pediatrics and neonatology·2026
Mental health in elite athletes: International Olympic Committee consensus statement (2026).
British journal of sports medicine·2026
Patient selection considerations for AADC deficiency gene therapy.
Annals of the Child Neurology Society·2026
GPIHBP1 Autoantibody-Related Hypertriglyceridemia in Children: A Report of Two Cases and a Review of Pediatric Cases From the Literature.
Molecular genetics & genomic medicine·2026
Optical Coherence Tomography Reflectivity as a Diagnostic Tool and Neurological Biomarker in Sialidosis Type I.
Journal of inherited metabolic disease·2026
Myopic Traction Maculopathy: consensus from the Myopia Society for a new nomenclature.
Ophthalmology. Retina·2026
Ocular Clues in Musculoskeletal Disorders: A Narrative Review for Orthopaedic Specialists.
Journal of the American Academy of Orthopaedic Surgeons. Global research & reviews·2026
Inferior oblique muscle branch incarceration in orbital floor trapdoor fractures: Clinical characteristics and the impact of surgical timing.
Journal of plastic, reconstructive & aesthetic surgery : JPRAS·2026
A Unique Case of Psychogenic Binocular Diplopia.
Case reports in ophthalmological medicine·2026