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Academic Journal

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

  • Authors : Pépin L; Department of Pediatric Endocrinology and Diabetology, University Hospital of Angers, Angers Cedex 9, France.; Colin E

Subjects: Endocrine System Diseases/Endocrine System Diseases/Endocrine System Diseases/*genetics ; Obesity/Obesity/Obesity/*genetics ; Proinsulin/Proinsulin/Proinsulin/*blood Proprotein Convertase 1 3 Deficiency

  • Source: The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2019 Apr 01; Vol. 104 (4), pp. 985-993.Publisher: Oxford University Press Country of Publication: United States NLM ID: 0375362 Publication Model: Print Cited Medium: Internet ISSN:

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  • 1-10 of  3,235 results for ""Endocrine System Diseases""