Lv2
130 积分 2025-10-23 加入
Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR
1个月前
已完结
Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR
1个月前
已完结
Myosin storage myopathy associated with a heterozygous missense mutation in MYH7
2个月前
已完结
Impaired chaperone-mediated autophagy leads to abnormal SORT1 (sortilin 1) turnover and CES1-dependent triglyceride hydrolysis
2个月前
已完结
2‐Ethylhexyl Diphenyl Phosphate Inhibited C2C12 Myoblast Differentiation by Regulating ACTC1
2个月前
已完结
Distal arthrogryposis and muscle weakness associated with a β-tropomyosin mutation
2个月前
已完结
Arthrogryposis in children: Etiological assessments and preparation of a protocol for etiological investigations
2个月前
已完结
Clinical and Genetic Findings in a Chinese Cohort of Dentatorubral–Pallidoluysian Atrophy Patients
2个月前
已完结
Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical Defects
3个月前
已完结
Human phenotype caused by biallelic KDM4B frameshift variant
3个月前
已完结
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