A New Case of PCSK1 Pathogenic Variant With Congenital Proprotein Convertase 1/3 Deficiency and Literature Review-Reference-Cited by-同舟云学术

A New Case of PCSK1 Pathogenic Variant With Congenital Proprotein Convertase 1/3 Deficiency and Literature Review

Author:

Pépin Lucie¹^ORCID,Colin Estelle²³,Tessarech Marine²³,Rouleau Stéphanie¹,Bouhours-Nouet Natacha¹⁴,Bonneau Dominique²³,Coutant Régis¹⁴

Affiliation:

1. Department of Pediatric Endocrinology and Diabetology, University Hospital of Angers, Angers Cedex 9, France

2. Department of Biochemistry and Genetics, University Hospital of Angers, Angers Cedex 9, France

3. UMR CNRS 6214-INSERM 1083 and PREMMI, University of Angers, Angers Cedex 9, France

4. Reference Center for Rare Diseases of Pituitary Origin—Constituent Site (HYPO), University Hospital of Angers, Angers Cedex 9, France

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

Reference32 articles.

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