Rare LPL gene missense mutation in an infant with hypertriglyceridemia

ConclusionsWe have here identified a rare pathogenic mutation in the LPL gene in a Chinese infant with severe hypertriglyceridemia.

Source: Journal of Clinical Laboratory Analysis - February 25, 2018 Category: Laboratory Medicine Authors: Yuan ‐yuan Qin, Ai‐qiu Wei, Qing‐wen Shan, Xiao‐ying Xian, Yang‐yang Wu, Lin Liao, Jie Yan, Zhan‐feng Lai, Fa‐quan Lin Tags: RESEARCH ARTICLE Source Type: research