Molecular genetics of phenylketonuria and tetrahydrobiopterin deficiency in Jordan-Reference-Cited by-同舟云学术

Molecular genetics of phenylketonuria and tetrahydrobiopterin deficiency in Jordan

Published:2020-05-19 Issue:1 Volume:55 Page:59-67
ISSN:2192-8312
Container-title:JIMD Reports
language:en
Short-container-title:JIMD Reports

Author:

Carducci Carla¹,Amayreh Wajdi²³,Ababneh Haneen³⁴,Mahasneh Amjad³⁴,Al Rababah Buthaina³,Al Qaqa Kefah²,Al Aqeel Momen²,Artiola Cristiana¹,Tolve Manuela¹,D'Amici Sirio¹,Shen Nan⁵,Yu Yongguo⁶,Hillert Alicia⁷,Himmelreich Nastassja⁷,Okun Jürgen G.⁷,Hoffmann Georg F.⁷,Blau Nenad⁷⁸

Affiliation:

1. Department of Experimental Medicine University of Rome “La Sapienza” Rome Italy

2. Queen Rania Children Hospital, King Hussein Medical Centre Amman Jordan

3. Princess Haya Biotechnology Centre Jordan University of Science and Technology Irbid Jordan

4. Department of Biotechnology and Genetic Engineering Jordan University of Science and Technology Irbid Jordan

5. Department of Rehabilitation Medicine Xin Hua Hospital affiliated to Shanghai Jiao Tong University School of Medicine Shanghai China

6. Department of Pediatric Endocrinology and Genetic Metabolism Shanghai Institute for Pediatric Research, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University Shanghai China

7. Dietmar Hopp Metabolic Center and Centre for Pediatrics and Adolescent Medicine University Hospital Heidelberg Heidelberg Germany

8. Division of Metabolism University Children's Hospital Zürich Switzerland

Funder

Jordan University of Science and Technology

Publisher

Wiley

Subject

Biochemistry, Genetics and Molecular Biology (miscellaneous),Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jmd2.12130

Reference23 articles.

1. Phenylketonuria