Correspondence on: "Discrepancy in Spinal Muscular Atrophy Incidence findings in newborn screening programs: the influence of carrier screening?" by Kay et al.

Dangouloff, Tamara; Boemer, François; Caberg, Jean-Hubert; Servais, Laurent

Dangouloff, Tamara; Boemer, François; Caberg, Jean-Hubert; Servais, Laurent.

Afiliação

Dangouloff T; Division of Child Neurology, Centre de Références des Maladies Neuromusculaires, Department of Pediatrics, University Hospital Liège & University of Liège, Liège, Belgium.
Boemer F; Biochemical Genetics Laboratory, Human Genetics Department, University Hospital Liège & University of Liège, Liège, Belgium.
Caberg JH; Molecular Genetics Laboratory, Human Genetics Department, University Hospital Liège & University of Liège, Liège, Belgium.
Servais L; Division of Child Neurology, Centre de Références des Maladies Neuromusculaires, Department of Pediatrics, University Hospital Liège & University of Liège, Liège, Belgium. laurent.servais@paediatrics.ox.ac.uk.

Genet Med ; 22(11): 1913-1914, 2020 11.

Article em En | MEDLINE | ID: mdl-32601389

Assuntos

Atrofia Muscular Espinal; Triagem Neonatal; Testes Genéticos; Humanos; Incidência; Recém-Nascido; Atrofia Muscular Espinal/diagnóstico; Atrofia Muscular Espinal/epidemiologia; Atrofia Muscular Espinal/genética

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Triagem Neonatal Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo

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XML

PubMed Links

Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Triagem Neonatal Idioma: En Ano de publicação: 2020 Tipo de documento: Article