Correspondence on: "Discrepancy in Spinal Muscular Atrophy Incidence findings in newborn screening programs: the influence of carrier screening?" by Kay et al
Genet Med. 2020 Nov;22(11):1913-1914.
doi: 10.1038/s41436-020-0887-1.
Epub 2020 Jun 30.
1 Division of Child Neurology, Centre de Références des Maladies Neuromusculaires, Department of Pediatrics, University Hospital Liège & University of Liège, Liège, Belgium.
2 Biochemical Genetics Laboratory, Human Genetics Department, University Hospital Liège & University of Liège, Liège, Belgium.
3 Molecular Genetics Laboratory, Human Genetics Department, University Hospital Liège & University of Liège, Liège, Belgium.
4 Division of Child Neurology, Centre de Références des Maladies Neuromusculaires, Department of Pediatrics, University Hospital Liège & University of Liège, Liège, Belgium. [email protected].
5 MDUK Neuromuscular Centre, Department of Paediatrics, University of Oxford, Oxford, UK. [email protected].