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Mosaicism in tuberous sclerosis complex: Lowering the threshold for clinical reporting.
Ye, Zimeng; Lin, Sufang; Zhao, Xia; Bennett, Mark F; Brown, Natasha J; Wallis, Mathew; Gao, Xinyi; Sun, Li; Wu, Jiarui; Vedururu, Ravikiran; Witkowski, Tom; Gardiner, Fiona; Stutterd, Chloe; Duan, Jing; Mullen, Saul A; McGillivray, George; Bodek, Simon; Valente, Giulia; Reagan, Matthew; Yao, Yi; Li, Lin; Chen, Li; Boys, Amber; Adikari, Thiuni N; Cao, Dezhi; Hu, Zhanqi; Beshay, Victoria; Zhang, Victor W; Berkovic, Samuel F; Scheffer, Ingrid E; Liao, Jianxiang; Hildebrand, Michael S.
Afiliación
  • Ye Z; Epilepsy Research Centre, Department of Medicine, The University of Melbourne, Heidelberg, Victoria, Australia.
  • Lin S; Department of Neurology, Epilepsy Centre, Shenzhen Children's Hospital, Shenzhen, Guangdong Province, China.
  • Zhao X; Department of Neurology, Epilepsy Centre, Shenzhen Children's Hospital, Shenzhen, Guangdong Province, China.
  • Bennett MF; Epilepsy Research Centre, Department of Medicine, The University of Melbourne, Heidelberg, Victoria, Australia.
  • Brown NJ; Population Health and Immunity Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
  • Wallis M; Department of Medical Biology, The University of Melbourne, Parkville, Victoria, Australia.
  • Gao X; Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.
  • Sun L; Department of Paediatrics, Royal Children's Hospital, The University of Melbourne, Parkville, Victoria, Australia.
  • Wu J; Victorian Clinical Genetics Services, Royal Children's Hospital, Parkville, Victoria, Australia.
  • Vedururu R; Austin Health, Heidelberg, Victoria, Australia.
  • Witkowski T; Tasmania Clinical Genetics Service, Royal Hobart Hospital, Tasmania, Australia.
  • Gardiner F; School of Medicine, University of Tasmania, Tasmania, Australia.
  • Stutterd C; Menzies Institute for Medical Research, University of Tasmania, Tasmania, Australia.
  • Duan J; AmCare Genomics Laboratory, Guangzhou, Guangdong Province, China.
  • Mullen SA; AmCare Genomics Laboratory, Guangzhou, Guangdong Province, China.
  • McGillivray G; AmCare Genomics Laboratory, Guangzhou, Guangdong Province, China.
  • Bodek S; Molecular Diagnostic Pathology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
  • Valente G; Epilepsy Research Centre, Department of Medicine, The University of Melbourne, Heidelberg, Victoria, Australia.
  • Reagan M; Epilepsy Research Centre, Department of Medicine, The University of Melbourne, Heidelberg, Victoria, Australia.
  • Yao Y; Victorian Clinical Genetics Services, Royal Children's Hospital, Parkville, Victoria, Australia.
  • Li L; Austin Health, Heidelberg, Victoria, Australia.
  • Chen L; Department of Neurology, Epilepsy Centre, Shenzhen Children's Hospital, Shenzhen, Guangdong Province, China.
  • Boys A; Epilepsy Research Centre, Department of Medicine, The University of Melbourne, Heidelberg, Victoria, Australia.
  • Adikari TN; Austin Health, Heidelberg, Victoria, Australia.
  • Cao D; Victorian Clinical Genetics Services, Royal Children's Hospital, Parkville, Victoria, Australia.
  • Hu Z; Austin Health, Heidelberg, Victoria, Australia.
  • Beshay V; Austin Health, Heidelberg, Victoria, Australia.
  • Zhang VW; Department of Medicine, Peninsula Health, Monash University, Frankston, Victoria, Australia.
  • Berkovic SF; Department of Neurology, Epilepsy Centre, Shenzhen Children's Hospital, Shenzhen, Guangdong Province, China.
  • Scheffer IE; Department of Neurology, Epilepsy Centre, Shenzhen Children's Hospital, Shenzhen, Guangdong Province, China.
  • Liao J; Department of Neurology, Epilepsy Centre, Shenzhen Children's Hospital, Shenzhen, Guangdong Province, China.
  • Hildebrand MS; Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.
Hum Mutat ; 43(12): 1956-1969, 2022 12.
Article en En | MEDLINE | ID: mdl-36030538
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Esclerosis Tuberosa Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Esclerosis Tuberosa Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article