Lv1
46 积分 2026-06-16 加入
Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia
18小时前
待确认
Phenotype and genotype of autosomal dominant tubulointerstitial kidney disease in a Japanese cohort
3天前
已完结
A SEC61A1 variant is associated with autosomal dominant polycystic liver disease
9天前
已完结
Exploring the ER channel protein Sec61: recent advances in pathophysiological significance and novel pharmacological inhibitors
11天前
已完结
Identification of a Novel De Novo Heterozygous SEC61A1 Variant in a Patient With Severe Congenital Neutropenia
11天前
已完结
Quantifying clinical and genetic factors influencing rate and severity of autosomal dominant tubulointerstitial kidney disease progression
12天前
已完结
Identification of a Novel De Novo Heterozygous SEC61A1 Variant in a Patient With Severe Congenital Neutropenia
18天前
已完结
Exploring the ER channel protein Sec61: recent advances in pathophysiological significance and novel pharmacological inhibitors
19天前
已完结
A SEC61A1 variant is associated with autosomal dominant polycystic liver disease
24天前
已完结
Autosomal dominant tubulointerstitial kidney disease in Chinese patients
27天前
已完结
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