A case of familial hypercholesterolemia caused by homozygous deletion in the LDLR gene diagnosed by targeted next-generation sequencing. Issue 1 (1st January 2019)

Record Type:
Journal Article
Title:
A case of familial hypercholesterolemia caused by homozygous deletion in the LDLR gene diagnosed by targeted next-generation sequencing. Issue 1 (1st January 2019)
Main Title:
A case of familial hypercholesterolemia caused by homozygous deletion in the LDLR gene diagnosed by targeted next-generation sequencing
Authors:
Melinkeri, Rashida Patanwala
Agarwal, Meenal
Anand, Siddharth
Sawant, Vishal A.
Singla, Ritu
Abstract:
Is Part Of:
Clinical lipidology and metabolic disorders. Volume 14:Issue 1(2019)
Journal:
Clinical lipidology and metabolic disorders
Issue:
Volume 14:Issue 1(2019)
Issue Display:
Volume 14, Issue 1 (2019)
Year:
2019
Volume:
14
Issue:
1
Issue Sort Value:
2019-0014-0001-0000
Page Start:
11
Page End:
16
Publication Date:
2019-01-01
Subjects:
Familial -- homozygous -- hypercholesterolemia -- deletion -- LDLR gene -- exon-9
Lipids -- Metabolism -- Disorders -- Periodicals
Lipids -- Metabolism -- Disorders
Lipid Metabolism Disorders
Metabolic Diseases
Electronic journals
Periodicals
571.9457
Journal URLs:
https://www.tandfonline.com/toc/tlip/current ↗
http://www.tandfonline.com/ ↗
DOI:
10.1080/26415321.2019.1670555 ↗
Languages:
English
ISSNs:
2641-5321
Deposit Type:
Legaldeposit
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:
12714.xml