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FMR1 mRNA from full mutation alleles is associated with ABC-CFX scores in males with fragile X syndrome.
Baker, Emma K; Arpone, Marta; Kraan, Claudine; Bui, Minh; Rogers, Carolyn; Field, Michael; Bretherton, Lesley; Ling, Ling; Ure, Alexandra; Cohen, Jonathan; Hunter, Matthew F; Santa María, Lorena; Faundes, Victor; Curotto, Bianca; Morales, Paulina; Trigo, Cesar; Salas, Isabel; Alliende, Angelica; Amor, David J; Godler, David E.
Afiliación
  • Baker EK; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, 50 Flemington Road, Parkville, VIC, 3052, Australia.
  • Arpone M; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, VIC, Australia.
  • Kraan C; School of Psychology and Public Health, La Trobe University, Bundoora, VIC, Australia.
  • Bui M; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, 50 Flemington Road, Parkville, VIC, 3052, Australia.
  • Rogers C; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, VIC, Australia.
  • Field M; Brain and Mind, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC, Australia.
  • Bretherton L; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, 50 Flemington Road, Parkville, VIC, 3052, Australia.
  • Ling L; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, VIC, Australia.
  • Ure A; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Carlton, VIC, Australia.
  • Cohen J; Genetics of Learning Disability Service, Hunter Genetics, Hunter New England Health, Waratah, NSW, Australia.
  • Hunter MF; Genetics of Learning Disability Service, Hunter Genetics, Hunter New England Health, Waratah, NSW, Australia.
  • Santa María L; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, 50 Flemington Road, Parkville, VIC, 3052, Australia.
  • Faundes V; Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, 50 Flemington Road, Parkville, VIC, 3052, Australia.
  • Curotto B; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, VIC, Australia.
  • Morales P; Neurodisability and Rehabilitation, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC, Australia.
  • Trigo C; Royal Children's Hospital, Melbourne, VIC, Australia.
  • Salas I; Department of Pediatrics, Monash University, Clayton, VIC, Australia.
  • Alliende A; Fragile X Alliance Inc, North Caulfield, VIC, Australia.
  • Amor DJ; Centre for Developmental Disability Health Victoria, Monash University, Clayton, VIC, Australia.
  • Godler DE; Monash Genetics, Monash Health, Clayton, VIC, Australia.
Sci Rep ; 10(1): 11701, 2020 07 16.
Article en En | MEDLINE | ID: mdl-32678152
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proyectos de Investigación / ARN Mensajero / Alelos / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Síndrome del Cromosoma X Frágil / Mosaicismo Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Humans / Male País/Región como asunto: America do sul / Chile / Oceania Idioma: En Revista: Sci Rep Año: 2020 Tipo del documento: Article País de afiliación: Australia
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proyectos de Investigación / ARN Mensajero / Alelos / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Síndrome del Cromosoma X Frágil / Mosaicismo Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Humans / Male País/Región como asunto: America do sul / Chile / Oceania Idioma: En Revista: Sci Rep Año: 2020 Tipo del documento: Article País de afiliación: Australia