Analysis of X‐inactivation status in a Rett syndrome natural history study cohort

Author:

Fang Xiaolan1ORCID,Butler Kameryn M.1,Abidi Fatima1,Gass Jennifer2,Beisang Arthur3,Feyma Timothy3,Ryther Robin C.4,Standridge Shannon56,Heydemann Peter7,Jones Mary8,Haas Richard9,Lieberman David N10,Marsh Eric D.11,Benke Tim A.12,Skinner Steve1,Neul Jeffrey L.13,Percy Alan K.14,Friez Michael J.1,Caylor Raymond C.1ORCID

Affiliation:

1. Greenwood Genetic Center Greenwood South Carolina USA

2. Florida Cancer Specialists & Research Institute Fort Myers FL USA

3. Gillette Children’s Specialty Healthcare St. Paul Minnesota USA

4. Department of Neurology Washington University School of Medicine St. Louis Missouri USA

5. Division of Neurology Cincinnati Children’s Hospital Medical Center Cincinnati Ohio USA

6. Department of Pediatrics, College of Medicine University of Cincinnati Cincinnati Ohio USA

7. Rush University Medical Center Chicago Illinois USA

8. Oakland Children’s Hospital, UCSF Oakland California USA

9. University of California San Diego San Diego California USA

10. Department of Neurology Boston Children’s Hospital Boston Massachusetts USA

11. Children’s Hospital of Philadelphia and University of Pennsylvania Philadelphia Pennsylvania USA

12. University of Colorado School of Medicine, Children’s Hospital Colorado‐Aurora Denver Colorado USA

13. Vanderbilt Kennedy Center Vanderbilt University Medical Center Nashville TN

14. The University of Alabama at Birmingham Birmingham Alabama USA

Funder

National Institutes of Health

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

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