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Mutations E688K and G569R within the <em>NALP3 </em>gene, associated with development of hereditary auto inflammatory disorders
Different mutations within the NALP3 gene are thought to be associated with development of several types of hereditary auto inflammatory disorders such as neonatal onset multisystem inflammatory disorder (NOMID) and muckle-wells syndrome (MWS). In this work two separate mutations E688K and G569R were supposed to be constructed by site-directed mutagenesis in the cloned wild type NA…
Contributors
- Ejdebäck Mikael Universitetslektor
- Nilsson Patric Universitetslektor
- Högskolan i Skövde Institutionen för vård och natur
Creator
- Fetah Alija 1967- , Högskolan i Skövde, Institutionen för vård och natur
Type of item
- Student thesis
- book
- Book
Date
- 2009
- 2010-09-20
- 2010-09-20
- 2009
Contributors
- Ejdebäck Mikael Universitetslektor
- Nilsson Patric Universitetslektor
- Högskolan i Skövde Institutionen för vård och natur
Creator
- Fetah Alija 1967- , Högskolan i Skövde, Institutionen för vård och natur
Type of item
- Student thesis
- book
- Book
Date
- 2009
- 2010-09-20
- 2010-09-20
- 2009
Providing institution
Aggregator
Rights statement for the media in this item (unless otherwise specified)
- http://rightsstatements.org/vocab/InC/1.0/
- http://rightsstatements.org/vocab/InC/1.0/
Identifier
- oai:DiVA.org:his-4246
Format
- electronic22
- electronic
- 22
Language
- en
- -1
Is part of
- http://data.theeuropeanlibrary.org/Collection/a1041
Year
- 2009
Providing country
- Sweden
Collection name
First time published on Europeana
- 2014-09-07T11:06:48.208Z
Last time updated from providing institution
- 2014-09-07T11:06:48.208Z