POLD1Germline Mutations in Patients Initially Diagnosed with Werner Syndrome

Author:

Lessel Davor1,Hisama Fuki M.2,Szakszon Katalin3,Saha Bidisha4,Sanjuanelo Alexander Barrios5,Salbert Bonnie A.6,Steele Pamela D.6,Baldwin Jennifer7,Brown W. Ted8,Piussan Charles9,Plauchu Henri10,Szilvássy Judit11,Horkay Edit12,Högel Josef13,Martin George M.4,Herr Alan J.4,Oshima Junko4,Kubisch Christian1

Affiliation:

1. Institute of Human Genetics; University Medical Center Hamburg-Eppendorf; Hamburg Germany

2. Division of Medical Genetics; Department of Medicine; University of Washington; Seattle Washington

3. Department of Pediatrics; University of Debrecen; Debrecen Hungary

4. Department of Pathology; University of Washington; Seattle Washington

5. Department of Medicine; Universidad Del Norte-CINPE Group; Barranquilla Colombia

6. Geisinger Medical Center; Danville Pennsylvania

7. Department of Dermatology; University of Minnesota; Minnesota

8. New York State Institute for Basic Research in Developmental Disabilities; Staten Island New York

9. Pediatric Genetics; University of Amiens; Amiens France

10. Département de Génétique; Université Claude Bernard Lyon 1 et Hôpital Louis Pradel; Hospices Civils de Lyon; F-69977 Bron CEDEX France

11. Department of Oto-Laryngology and Head and Neck Surgery; University of Debrecen; Debrecen Hungary

12. Diagnoscan Hungary; Debrecen Hungary

13. Institute of Human Genetics; University of Ulm; Ulm Germany

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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