{"id":1156,"date":"2021-05-05T09:21:59","date_gmt":"2021-05-05T06:21:59","guid":{"rendered":"https:\/\/sites.uef.fi\/genediagnostics\/?page_id=1156"},"modified":"2022-05-05T10:35:10","modified_gmt":"2022-05-05T07:35:10","slug":"nephrotic-syndrome","status":"publish","type":"page","link":"https:\/\/sites.uef.fi\/genediagnostics\/monogenic-diseases\/nephrotic-syndrome\/?lang=en","title":{"rendered":"Nephrotic syndrome"},"content":{"rendered":"<h1><strong>Nephrotic syndrome<\/strong><\/h1>\n<p>Sequencing of the coding region of the NPHS2 gene.<\/p>\n<p>The analysis is performed from a whole blood sample (EDTA). Instructions for storage and sending the sample as well as prices for DNA screening are given in the request form. The report and interpretation of the results are mailed to the address given in the order 6-8 weeks after the arrival of the blood sample.<\/p>\n<p><a href=\"https:\/\/sites.uef.fi\/genediagnostics\/wp-content\/uploads\/sites\/100\/2022\/05\/NPHS2_Genetic_analysis.pdf\">Request form<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Nephrotic syndrome Sequencing of the coding region of the NPHS2 gene. The analysis is performed from a whole blood sample (EDTA). Instructions for storage and sending the sample as well as prices for DNA screening are given in the request form. The report and interpretation of the results are mailed to the address given in [&hellip;]<\/p>\n","protected":false},"author":203,"featured_media":514,"parent":271,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"class_list":["post-1156","page","type-page","status-publish","has-post-thumbnail","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.1.1 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Nephrotic syndrome - Geenidiagnostiikka<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/sites.uef.fi\/genediagnostics\/monogenic-diseases\/nephrotic-syndrome\/?lang=en\" \/>\n<meta property=\"og:locale\" content=\"fi_FI\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Nephrotic syndrome - Geenidiagnostiikka\" \/>\n<meta property=\"og:description\" content=\"Nephrotic syndrome Sequencing of the coding region of the NPHS2 gene. The analysis is performed from a whole blood sample (EDTA). Instructions for storage and sending the sample as well as prices for DNA screening are given in the request form. 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