Lv1
26 积分 2022-06-27 加入
Risk factors for early-onset and late-onset dementia: a prospective cohort study
4天前
已完结
Whole-exome sequencing for diagnosis of hereditary ichthyosis
8天前
已完结
Next-generation sequencing through multi-gene panel testing for diagnosis of hereditary ichthyosis in Chinese
8天前
已完结
Arrhythmogenesis in a Novel Murine Model with KCNJ2 Mutation of Familial Atrial Fibrillation
22天前
已完结
Atrial proarrhythmia due to increased inward rectifier current (IK1) arising from KCNJ2 mutation – A simulation study
22天前
已完结
Manifestation, Management and Molecular Analysis of Candidate Genes in Two Rare Cases of Thyrotoxic Hypokalemic Periodic Paralysis
22天前
已完结
Vitamin C inhibits ACSL4 to alleviate ferro-aging in primates
1个月前
已完结
Molecular genetic analysis of 30 families with Joubert syndrome
1个月前
已完结
Generative AI: a partner for genetic counseling?
2个月前
已完结
R1193Q of SCN5A, a Brugada and long QT mutation, is a common polymorphism in Han Chinese
3个月前
已完结
皖公网安备34019202002308
