Exome sequencing identifies a de novo FOXA2 variant in a patient with syndromic diabetes-Reference-Cited by-同舟云学术

Exome sequencing identifies a de novo FOXA2 variant in a patient with syndromic diabetes

Author:

Stekelenburg Caroline¹²,Gerster Karine³,Blouin Jean‐Louis⁴⁵,Lang‐Muritano Mariarosaria³⁶,Guipponi Michel⁵,Santoni Federico⁷,Schwitzgebel Valerie M.¹²

Affiliation:

1. Pediatric Endocrine and Diabetes Unit, Department of PediatricsUniversity Hospitals of Geneva Geneva Switzerland

2. Diabetes Center of the Faculty of MedicineUniversity of Geneva Geneva Switzerland

3. Division of Pediatric Endocrinology and DiabetologyUniversity Children's Hospital Zurich Switzerland

4. Department of Genetic Medicine and Development, Faculty of MedicineUniversity of Geneva Geneva Switzerland

5. Department of Genetic Medicine and LaboratoryUniversity Hospitals of Geneva Geneva Switzerland

6. Children's Research CenterUniversity Children's Hospital Zurich Switzerland

7. Department of Medicine—Service of Endocrinology, Diabetes and MetabolismUniversity Hospitals of Lausanne Lausanne Switzerland

Funder

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health,Internal Medicine

Link

Reference17 articles.

2. Precision medicine for monogenic diabetes: from a survey to the development of a next‐generation diagnostic panel;Kherra S;Swiss Med Wkly,2017

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