KFU. Card publication. Rare regulatory variant in the MEF2D gene is associated with SLE in Swedish patients and contributes to the gene regulation and splicing

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RARE REGULATORY VARIANT IN THE MEF2D GENE IS ASSOCIATED WITH SLE IN SWEDISH PATIENTS AND CONTRIBUTES TO THE GENE REGULATION AND SPLICING

Form of presentation

Articles in international journals and collections

Year of publication

2019

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Authors, employees of KFU

Abramov Sergey Nikolaevich, author

Bibliographic description in the original language

Kozyrev S. V., Farias F. H. G., Dahlqvist J., Rare regulatory variant in the MEF2D gene is associated with SLE in Swedish patients and contributes to the gene regulation and splicing//EUROPEAN JOURNAL OF HUMAN GENETICS. - 2019. - Vol.27, Is.. - P.207-208.

Keywords

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The name of the journal

European Journal of Human Genetics

Please use this ID to quote from or refer to the card

https://repository.kpfu.ru/eng/?p_id=221355&p_lang=2

Full metadata record

Field DC	Value	Language
dc.contributor.author	Abramov Sergey Nikolaevich	ru_RU
dc.date.accessioned	2019-01-01T00:00:00Z	ru_RU
dc.date.available	2019-01-01T00:00:00Z	ru_RU
dc.date.issued	2019	ru_RU
dc.identifier.citation	Kozyrev S. V., Farias F. H. G., Dahlqvist J., Rare regulatory variant in the MEF2D gene is associated with SLE in Swedish patients and contributes to the gene regulation and splicing//EUROPEAN JOURNAL OF HUMAN GENETICS. - 2019. - Vol.27, Is.. - P.207-208.	ru_RU
dc.identifier.uri	https://repository.kpfu.ru/eng/?p_id=221355&p_lang=2	ru_RU
dc.description.abstract	European Journal of Human Genetics	ru_RU
dc.language.iso	ru	ru_RU
dc.subject		ru_RU
dc.title	Rare regulatory variant in the MEF2D gene is associated with SLE in Swedish patients and contributes to the gene regulation and splicing	ru_RU
dc.type	Articles in international journals and collections	ru_RU