URAT1 mutations cause renal hypouricaemia combined with Fanconi syndrome in a Chinese patient. Issue 8 (29th July 2018)

Record Type:: Journal Article
Title:: URAT1 mutations cause renal hypouricaemia combined with Fanconi syndrome in a Chinese patient. Issue 8 (29th July 2018)
Main Title:: URAT1 mutations cause renal hypouricaemia combined with Fanconi syndrome in a Chinese patient
Authors:: Du, Juan
Jiang, Yan
Wang, Ou
Li, Mei
Xing, Xiao‐Ping
Xia, Weibo
Abstract:
Is Part Of:: Nephrology. Volume 23:Issue 8(2018)
Journal:: Nephrology
Issue:: Volume 23:Issue 8(2018)
Issue Display:: Volume 23, Issue 8 (2018)
Year:: 2018
Volume:: 23
Issue:: 8
Issue Sort Value:: 2018-0023-0008-0000
Page Start:: 797
Page End:: 798
Publication Date:: 2018-07-29
Subjects:: Nephrology -- Periodicals
Kidneys -- Diseases -- Periodicals
Nephrologists -- Periodicals
616.61
616.61
Journal URLs:: http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/nep.13190 ↗
Languages:: English
ISSNs:: 1320-5358
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 6075.684400
British Library DSC - BLDSS-3PM
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Ingest File:: 7060.xml