Recurrent recessive mutation in deoxyguanosine kinase causes idiopathic noncirrhotic portal hypertension

Author:

Vilarinho Sílvia12,Sari Sinan3,Yilmaz Güldal4,Stiegler Amy L.5,Boggon Titus J.56,Jain Dhanpat127,Akyol Gulen4,Dalgic Buket3,Günel Murat289,Lifton Richard P.2910

Affiliation:

1. Department of Internal Medicine, Section of Digestive Diseases; Yale University School of Medicine; New Haven CT

2. Department of Genetics; Yale University School of Medicine; New Haven CT

3. Department of Pediatrics, Division of Gastroenterology; Gazi University, Faculty of Medicine; Ankara Turkey

4. Department of Pathology; Gazi University, Faculty of Medicine; Ankara Turkey

5. Department of Pharmacology; Yale University School of Medicine; New Haven CT

6. Department of Molecular Biophysics and Biochemistry; Yale University; New Haven CT

7. Department of Pathology; Yale University School of Medicine; New Haven CT

8. Department of Neurosurgery, Yale Program in Brain Tumor Research; Yale University School of Medicine; New Haven CT

9. Yale Center for Mendelian Genomics; Yale University School of Medicine; New Haven CT

10. Department of Internal Medicine and Howard Hughes Medical Institute; Yale University School of Medicine; New Haven CT

Funder

US National Institutes of Health, Centers for Mendelian Genomics

Publisher

Wiley

Subject

Hepatology

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