Expanding the spectrum of CEP55 ‐associated disease to viable phenotypes

Author:

Barrie Elizabeth S.1ORCID,Overwater Eline2,Haelst Mieke M.2,Motazacker M. Mahdi3,Truxal Kristen V.45,Crist Erin1,Mostafavi Roya6,Pivnick Eniko K.7,Choudhri Asim F.8,Narumanchi TaraChandra9,Castelluccio Valerie10ORCID,Walsh Laurence E.11,Garganta Cheryl12,Gastier‐Foster Julie M.113

Affiliation:

1. The Institute for Genomic Medicine, Nationwide Children's Hospital Columbus Ohio

2. Department of Clinical Genetics, Amsterdam UMCUniversity of Amsterdam Amsterdam The Netherlands

3. Laboratory of Genome Diagnostics, Amsterdam UMC, University of Amsterdam Amsterdam Netherlands

4. Division of Genetic and Genomic MedicineNationwide Children's Hospital Columbus Ohio

5. Department of PediatricsThe Ohio State University College of Medicine Columbus Ohio

6. Department of OncologySt. Jude Children's Research Hospital Memphis Tennessee

7. Department of Pediatrics and OphthalmologyUniversity of Tennessee Health Science Center Memphis Tennessee

8. Department of Radiology, Ophthalmology, and NeurosurgeryUniversity of Tennessee Health Science Center Memphis Tennessee

9. Department of PediatricsWest Virginia University Morgantown West Virginia

10. Department of Medical and Molecular GeneticsIndiana University School of Medicine Indianapolis Indiana

11. Department of Neurology, Medical and Molecular Genetics, and PediatricsIndiana University School of Medicine Indianapolis Indiana

12. Department of Pediatrics, Division of Genetics and MetabolismUniversity of Florida Gainesville Florida

13. Department of Pathology and PediatricsThe Ohio State University College of Medicine Columbus Ohio

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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