LPL gene mutation as the cause of severe hypertriglyceridemia in the course of ketoacidosis in a patient with newly diagnosed type 1 diabetes mellitus

Julita Nocoń-Bohusz; Beata Wikiera; Aleksander Basiak; Robert Śmigiel; Anna Noczyńska

eISSN: 2083-8441
ISSN: 2081-237X

Pediatric Endocrinology Diabetes and Metabolism

Current issue Archive Manuscripts accepted About the journal Editorial board Reviewers Abstracting and indexing Subscription Contact Ethical standards and procedures Supplements Instructions for authors Publication charge

Editorial System

Submit your Manuscript

Editorial Policies

Sarajevo Declaration on Integrity and Visibility of Scholarly Publications

Open access

Journal integrated with

2/2015
vol. 21

Send email

Copy url:

Case report

LPL gene mutation as the cause of severe hypertriglyceridemia in the course of ketoacidosis in a patient with newly diagnosed type 1 diabetes mellitus

Julita Nocoń-Bohusz

,

Beata Wikiera

,

Aleksander Basiak

,

Robert Śmigiel

,

Anna Noczyńska

Pediatr Endocrinol Diabetes Metab 2015;21,2:89-92

Online publish date: 2016/02/18

Article file

- a_36570.pdf [0.82 MB]

Get citation

LPL gene mutation as the cause of severe hypertriglyceridemia in the course of ketoacidosis in a patient with newly diagnosed type 1 diabetes mellitus

Julita Nocoń-Bohusz , Beata Wikiera , Aleksander Basiak , Robert Śmigiel , Anna Noczyńska

Julita Nocoń-Bohusz

,

Beata Wikiera

,

Aleksander Basiak

,

Robert Śmigiel

,

Anna Noczyńska