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Prenatal mucopolysaccharidosis VII: A novel pathogenic variant identified in GUSB gene.
Poyatos-Andújar, Antonio Miguel; García-Linares, Susana; Carretero, Pilar; Ocon, Olga; Fresneda, Dolores; Gort, Laura; Molina García, Francisa Sonia.
Afiliação
  • Poyatos-Andújar AM; UGC de Laboratorios Laboratorio de Genética Hospital Universitario San Cecilio Granada Spain.
  • García-Linares S; UGC de Laboratorios Laboratorio de Genética Hospital Universitario San Cecilio Granada Spain.
  • Carretero P; Department of Obstetrics and Gynecology Hospital Universitario San Cecilio Instituto de Investigación Biosanitaria IBS Granada Spain.
  • Ocon O; Department of Obstetrics and Gynecology Hospital Universitario San Cecilio Instituto de Investigación Biosanitaria IBS Granada Spain.
  • Fresneda D; Department of Obstetrics and Gynecology Hospital Universitario San Cecilio Instituto de Investigación Biosanitaria IBS Granada Spain.
  • Gort L; Secció d'Errors Congènits del Metabolisme -IBC Servei de Bioquímica i Genètica Molecular Hospital Clínic IDIBAPS, CIBERER Barcelona Spain.
  • Molina García FS; Department of Obstetrics and Gynecology Hospital Universitario San Cecilio Instituto de Investigación Biosanitaria IBS Granada Spain.
Clin Case Rep ; 9(2): 790-795, 2021 Feb.
Article em En | MEDLINE | ID: mdl-33598246
Clinical exome sequencing is a powerful approach to overcome the wide clinical and genetic heterogeneity of mucopolysaccharidosis. These data could be useful for prenatal diagnosis of MPS VII, genetic counseling, and preimplantation genetic testing.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Clin Case Rep Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Clin Case Rep Ano de publicação: 2021 Tipo de documento: Article