טוען...
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...
שמור ב:
| Main Authors: | , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2008
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| נושאים: | |
| גישה מקוונת: | 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 |
| תגים: |
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