Genetic variants in the ITPR2 gene are associated with Kashin‐Beck Disease in Tibetan
Genetic variants in the ITPR2 gene are associated with Kashin‐Beck Disease in Tibetan
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ITPR2基因的遗传变异与藏族大骨节病有关
DOI:
10.1002/mgg3.715
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发表时间:
2019-05
期刊:
影响因子:
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通讯作者:
Tianbo Jin
中科院分区:
文献类型:
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作者:
Xue He;Mei Bai;Ming Liu;Li Wang;Yongjun He;Hao Rong;Dongya Yuan;Tianbo Jin
Kashin‐Beck Disease (KBD) is a chronic, endemic osteoarthropathy. Inositol 1,4,5‐triphosphate receptor type 2 (ITPR2) gene is involved in chondrocytes. We speculated that single‐nucleotide polymorphisms (SNPs) in ITPR2 gene may have an association with KB
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影响因子:
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通讯作者:
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影响因子:
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