Identification and functional characterization of mutations in LPL gene causing severe hypertriglyceridaemia and acute pancreatitis-Reference-Cited by-同舟云学术

Identification and functional characterization of mutations in LPL gene causing severe hypertriglyceridaemia and acute pancreatitis

Published:2020-01 Issue:2 Volume:24 Page:1286-1299
ISSN:1582-1838
Container-title:Journal of Cellular and Molecular Medicine
language:en
Short-container-title:J Cell Mol Med

Author:

Han Peng¹²,Wei Guohong³,Cai Ke³,Xiang Xi²⁴⁵,Deng Wang Ping³,Li Yan Bing³,Kuang Shan¹²,Dong Zhanying¹²,Zheng Tianyu¹²⁵,Luo Yonglun¹²⁴⁶,Liu Junnian¹²⁴,Guan Yuanning¹²,Li Chen⁷,Dey Subrata Kumar⁸⁹,Liao Zhihong³,Banerjee Santasree¹²⁴⁹^ORCID

Affiliation:

1. BGI‐Qingdao BGI‐Shenzhen Qingdao China

2. China National GeneBank BGI‐Shenzhen Shenzhen China

3. Department of Endocrinology The First Affiliated Hospital of Sun Yat‐sen University Guangzhou China

4. BGI‐Shenzhen Shenzhen China

5. BGI Education Center University of Chinese Academy of Sciences Shenzhen China

6. Department of Biomedicine Aarhus University Aarhus Denmark

7. Institute of Genetics and Department of Genetics Zhejiang University School of Medicine Hangzhou China

8. Department of Biotechnology Centre for Genetic Studies School of Biotechnology and Biological Sciences Maulana Abul Kalam Azad University of Technology (Formerly West Bengal University of Technology) Kolkata India

9. Brainware university Barasat West Bengal India

Funder

Guangzhou Science and Technology Programme

Publisher

Wiley

Subject

Cell Biology,Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jcmm.14768

Reference32 articles.

1. Hypertriglyceridemia

2. Acute pancreatitis patient registry to examine novel therapies in clinical experience (APPRENTICE): an international, multicenter consortium for the study of acute pancreatitis;Papachristou GI;Ann Gastroenterol,2017

3. Hypertriglyceridemic Pancreatitis: Presentation and Management

4. Evaluation and Treatment of Hypertriglyceridemia: An Endocrine Society Clinical Practice Guideline

5. Current knowledge of hypertriglyceridemic pancreatitis

Cited by 62 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinical and genetic characteristics of Chinese patients with congenital fibrosis of the extraocular muscles;Orphanet Journal of Rare Diseases;2024-08-15

2. A novel mutation in the ATP7B gene causing hepatolenticular degeneration in a Chinese family: A case report;Medicine;2024-08-02

3. Novel splice site and nonsense variants in PKHD1 cause autosomal recessive polycystic kidney disease in a Chinese Zhuang ethnic family;Medicine;2024-08-02

4. Chinese carrier of the HNF1A p.Gln444fs variant exhibits enhanced response to sulfonylureas;Heliyon;2024-08

5. A Novel RP1 Truncating mutation That Causes Autosomal Dominant Retinitis Pigmentosa (ADRP);Advances in Ophthalmology Practice and Research;2024-08