Identification of a dysfunctional splicing mutation in the SLC22A12/URAT1 gene causing renal hypouricaemia type 1: a report on two families. (4th October 2020)

Record Type:: Journal Article
Title:: Identification of a dysfunctional splicing mutation in the SLC22A12/URAT1 gene causing renal hypouricaemia type 1: a report on two families. (4th October 2020)
Main Title:: Identification of a dysfunctional splicing mutation in the SLC22A12/URAT1 gene causing renal hypouricaemia type 1: a report on two families
Authors:: Kawamura, Yusuke
Toyoda, Yu
Ohnishi, Takuma
Hisatomi, Ryutaro
Higashino, Toshihide
Nakayama, Akiyoshi
Shimizu, Seiko
Yanagi, Masato
Kamimaki, Isamu
Fujimaru, Rika
Suzuki, Hiroshi
Shinomiya, Nariyoshi
Takada, Tappei
Matsuo, Hirotaka
Abstract:
Is Part Of:: Rheumatology. Volume 59:Number 12(2020)
Journal:: Rheumatology
Issue:: Volume 59:Number 12(2020)
Issue Display:: Volume 59, Issue 12 (2020)
Year:: 2020
Volume:: 59
Issue:: 12
Issue Sort Value:: 2020-0059-0012-0000
Page Start:: 3988
Page End:: 3990
Publication Date:: 2020-10-04
Subjects:: Rheumatism -- Periodicals
Rheumatology -- Periodicals
616.723005
Journal URLs:: http://rheumatology.oupjournals.org ↗
http://rheumatology.oxfordjournals.org ↗
http://ukcatalogue.oup.com/ ↗
http://firstsearch.oclc.org ↗
DOI:: 10.1093/rheumatology/keaa461 ↗
Languages:: English
ISSNs:: 1462-0324
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 7960.731900
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Ingest File:: 15236.xml