Detection of Novel Gene Variants Associated with Congenital Hypothyroidism in a Finnish Patient Cohort

Author:

Löf Christoffer1,Patyra Konrad1,Kuulasmaa Teemu2,Vangipurapu Jagadish2,Undeutsch Henriette1,Jaeschke Holger1,Pajunen Tuulia1,Kero Andreina1,Krude Heiko3,Biebermann Heike3,Kleinau Gunnar3,Kühnen Peter3,Rantakari Krista4,Miettinen Päivi4,Kirjavainen Turkka4,Pursiheimo Juha-Pekka5,Mustila Taina6,Jääskeläinen Jarmo6,Ojaniemi Marja7,Toppari Jorma18,Ignatius Jaakko9,Laakso Markku2,Kero Jukka18

Affiliation:

1. Department of Physiology, Institute of Biomedicine, University of Turku, Turku, Finland.

2. Faculty of Health Sciences, Institute of Clinical Medicine, Internal Medicine, University of Eastern Finland, Kuopio, Finland.

3. Institute of Experimental Pediatric Endocrinology, Charité Universitätsmedizin Berlin, Berlin, Germany.

4. Hospital for Children and Adolescents, Hospital District of Helsinki and Uusimaa, Helsinki, Finland.

5. Turku Clinical Sequencing Laboratory, Institute of Biomedicine, University of Turku, Turku, Finland.

6. Department of Pediatrics, Seinäjoki Central Hospital, Seinäjoki, Finland.

7. Department of Children and Adolescents, Oulu University Hospital, Oulu, Finland.

8. Department of Pediatrics, Turku University Hospital, Turku, Finland.

9. Department of Clinical Genetics, Turku University Hospital, Turku, Finland.

Publisher

Mary Ann Liebert Inc

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

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