Hereditas

Hereditas

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167

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Last Updated: Aug 05, 2025

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A novel mutation in the FGG gene causes hypofibrinogenemia in a Chinese family.

Xie X, Du J, Geng S, Yi B, Li Q, Zuo J.

2024 PMID: 38374144
3/7
COI Funding
COI Funding
COI Funding
Integrative single-cell analysis: dissecting CD8 + memory cell roles in LUAD and COVID-19 via eQTLs and Mendelian Rando…

Wu J, Mao X, Liu X, Mao J, Yang X, Zhou X, Tianzhu L, Ji Y, Li Z, Xu H.

2024 PMID: 38297377
3/7
COI Funding
Network pharmacology to unveil the mechanism of suanzaoren decoction in the treatment of alzheimer's with diabetes.

Chen T, Lei Y, Li M, Liu X, Zhang L, Cai F, Gong X, Zhang R.

2024 PMID: 38167125
3/7
COI Funding
COI Funding
COI Funding
COI Funding