Whole-Exome Sequencing Reveals a Rare Missense Variant in SLC16A9 in a Pedigree with Early-Onset Gout.

Autor: Huang, Xiu-Feng1 (AUTHOR), Sun, Li2 (AUTHOR), Zhang, Chunwu3 (AUTHOR), Zhou, Zhenni4 (AUTHOR), Chen, Hui5 (AUTHOR), Zhang, Linhua6 (AUTHOR), Brown, Matthew A.7,8 (AUTHOR), Xia, Xiaoru2 (AUTHOR)
Zdroj: BioMed Research International. 1/31/2020, p1-6. 6p.
Databáze: Academic Search Ultimate
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