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EXCLUSION OF HOMOZYGOUS PLCE1 (NPHS3) MUTATIONS IN 69 FAMILIES WITH IDIOPATHIC AND HEREDITARY FSGS
Focal and segmental glomerulosclerosis (FSGS) is the most common glomerular cause of end-stage kidney disease (ESKD). The etiology of FSGS has not been fully elucidated; recent results from the positional cloning of genes mutated in nephrotic syndromes are now beginning to provide insight into the p...
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| 主要な著者: | , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2008
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3070354/ https://ncbi.nlm.nih.gov/pubmed/18975016 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-008-1025-5 |
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