Screening of WT1 mutations in exon 8 and 9 in children with steroid resistant nephrotic syndrome from a single centre and establishment of a rapid screening assay using high-resolution melting analysis in a clinical setting.
| Autor: | Siji, Annes1, Pardeshi, Varsha Chhotusing1, Ravindran, Shilpa1, Vasudevan, Ambily1, Vasudevan, Anil1,2 anil.vasudevan@sjri.res.in |
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| Zdroj: | BMC Medical Genetics. 1/10/2017, Vol. 18, p1-10. 10p. |
| Databáze: | Academic Search Ultimate |
| Externí odkaz: |
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