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Nephrin - mutations in congenital nephrotic syndrome of the Finnish type and cell lineage specific gene regulation /

Diss. (sammanfattning) Stockholm : Karolinska institutet, 2005. / Hàˆrtill 3 uppsatser.

Identiferoai:union.ndltd.org:OCLC/oai:xtcat.oclc.org:OCLCNo/186777715
Date January 2005
CreatorsBeltcheva, Olga,
PublisherStockholm : Karolinska institutet,
Source SetsOCLC
LanguageEnglish
Detected LanguageEnglish
SourceOnline

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