Výsledky vyhledávání - "Ambily Vasudevan"

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: Annes Siji, V. C. Pardeshi, Ambily Vasudevan, Shilpa Ravindran, Anil Vasudevan

Publikováno v: BMC Medical Genetics

Background Mutations in Wilm’s tumor 1 (WT1) gene is one of the commonly reported genetic mutations in children with steroid resistant nephrotic syndrome (SRNS). We report the results of direct sequencing of exons 8 and 9 of WT1 gene in 100 childre

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a405acce8b1bcf7dd963cd8e13c88576
https://doi.org/10.1186/s12881-016-0362-7

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Additional file 2: Table S1. of 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: Annes Siji, Pardeshi, Varsha, Ravindran, Shilpa, Ambily Vasudevan, Vasudevan, Anil

Summary of the properties of High Resolution Melt and Direct sequencing. (DOCX 12Â kb)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19ea9d70f73ded42b836a3c77535349c

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