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370 积分 2024-04-20 加入
Ophthalmological Aspects of Pierson Syndrome
3个月前
已完结
[LAMB2 gene mutation as a cause of congenital nephrotic syndrome with distinct eye abnormalities and hypotonia]
3个月前
已关闭
Nephrotic Syndrome in the First Year of Life: Two Thirds of Cases Are Caused by Mutations in 4 Genes (NPHS1, NPHS2, WT1, and LAMB2)
3个月前
已完结
Collagen IV in Gould syndrome and Alport syndrome
4个月前
已完结
The laminin family
4个月前
已完结
Early-Onset Myopia and Retinal Detachment without Typical Microcoria or Severe Proteinuria due to a Novel LAMB2 Variant
5个月前
已完结
Molecular mechanisms determining severity in patients with Pierson syndrome
5个月前
已完结
Case Report of Nephrogenic Diabetes Insipidus with a Novel Mutation in the AQP2 Gene
5个月前
已完结
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