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Amplicon targeted resequencing for SLC2A9 and SLC22A12 identified novel mutations in hypouricemia subjects
BACKGROUND: To identify potential causative mutations in SLC2A9 and SLC22A12 that lead to hypouricemia or hyperuricemia (HUA). METHODS: Targeted resequencing of whole exon regions of SLC2A9 and SLC22A12 was performed in three cohorts of 31 hypouricemia, 288 HUA and 280 normal controls. RESULTS: A to...
Autores principales: | Zhou, Zhaowei, Wang, Ke, Zhou, Juan, Wang, Can, Li, Xinde, Cui, Lingling, Han, Lin, Liu, Zhen, Ren, Wei, Wang, Xuefeng, Zhang, Keke, Li, Zhiqiang, Pan, Dun, Li, Changgui, Shi, Yongyong |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625124/ https://www.ncbi.nlm.nih.gov/pubmed/31131560 http://dx.doi.org/10.1002/mgg3.722 |
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