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Article

SLC2A3 variants in familial and sporadic congenital heart diseases in a Chinese Yunnan population.

Journal of clinical laboratory analysis - 1 Jun 2022

Ma Lijing, Xu Jiaxin, Tang Qisheng, Cao Yu, Kong Ruize, Li Kunlin, Liu Jie, Jiang Lihong

Abstract excerpt

BACKGROUND: Solute carrier family 2 member 3 (SLC2A3), is a member of a superfamily of transport protein genes. SLC2A3 played an important role in embryonic development. Previous research reported SLC2A3 duplication was reportedly associated with congenital syndromic heart defects. However, it is not clear whether the gene is associated with non-syndromic congenital heart disease. Our study aimed to elucidate the...

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PMID: 35466476
DOI: 10.1002/jcla.24456
PMCID: PMC9169219

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