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FXN gene methylation determines carrier status in Friedreich ataxia.
Lam, Christina; Gilliam, Kaitlyn M; Rodden, Layne N; Schadt, Kimberly A; Lynch, David R; Bidichandani, Sanjay.
Afiliación
  • Lam C; Department of Pediatrics, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA.
  • Gilliam KM; Department of Pediatrics, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA.
  • Rodden LN; Department of Pediatrics, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA.
  • Schadt KA; Department of Neurology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Lynch DR; Department of Neurology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Bidichandani S; Department of Neurology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
J Med Genet ; 60(8): 797-800, 2023 08.
Article en En | MEDLINE | ID: mdl-36635061
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ataxia de Friedreich Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: J Med Genet Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ataxia de Friedreich Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: J Med Genet Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos