Mosaicism in tuberous sclerosis complex: Lowering the threshold for clinical reporting

Author:

Ye Zimeng1ORCID,Lin Sufang2,Zhao Xia2,Bennett Mark F.134,Brown Natasha J.567,Wallis Mathew891011,Gao Xinyi12,Sun Li12,Wu Jiarui12,Vedururu Ravikiran13,Witkowski Tom1,Gardiner Fiona1,Stutterd Chloe78,Duan Jing2,Mullen Saul A.18,McGillivray George7,Bodek Simon8,Valente Giulia8,Reagan Matthew14,Yao Yi2,Li Lin2,Chen Li2,Boys Amber5,Adikari Thiuni N.110,Cao Dezhi2,Hu Zhanqi2,Beshay Victoria13,Zhang Victor W.12,Berkovic Samuel F.18,Scheffer Ingrid E.156815,Liao Jianxiang2,Hildebrand Michael S.158

Affiliation:

1. Epilepsy Research Centre, Department of Medicine The University of Melbourne Heidelberg Victoria Australia

2. Department of Neurology Epilepsy Centre, Shenzhen Children's Hospital Shenzhen Guangdong Province China

3. Population Health and Immunity Division, The Walter and Eliza Hall Institute of Medical Research Parkville Victoria Australia

4. Department of Medical Biology The University of Melbourne Parkville Victoria Australia

5. Murdoch Children's Research Institute, Royal Children's Hospital Parkville Victoria Australia

6. Department of Paediatrics, Royal Children's Hospital The University of Melbourne Parkville Victoria Australia

7. Victorian Clinical Genetics Services, Royal Children's Hospital Parkville Victoria Australia

8. Austin Health Heidelberg Victoria Australia

9. Tasmania Clinical Genetics Service, Royal Hobart Hospital Tasmania Australia

10. School of Medicine University of Tasmania Tasmania Australia

11. Menzies Institute for Medical Research University of Tasmania Tasmania Australia

12. AmCare Genomics Laboratory Guangzhou Guangdong Province China

13. Molecular Diagnostic Pathology, Peter MacCallum Cancer Centre Melbourne Victoria Australia

14. Department of Medicine, Peninsula Health Monash University Frankston Victoria Australia

15. The Florey Institute Parkville Victoria Australia

Funder

Epilepsy Foundation of Victoria

Sanming Project of Medicine in Shenzhen

Publisher

Hindawi Limited

Subject

Genetics (clinical),Genetics

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