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Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia
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title
Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia
(English)
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main subject
glucose
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author name string
Hirotaka Matsuo
series ordinal
1
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Toshinori Chiba
series ordinal
2
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Shushi Nagamori
series ordinal
3
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Akiyoshi Nakayama
series ordinal
4
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Hideharu Domoto
series ordinal
5
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Kanokporn Phetdee
series ordinal
6
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Pattama Wiriyasermkul
series ordinal
7
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Yuichi Kikuchi
series ordinal
8
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Takashi Oda
series ordinal
9
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Junichiro Nishiyama
series ordinal
10
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Takahiro Nakamura
series ordinal
11
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Yuji Morimoto
series ordinal
12
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Keiko Kamakura
series ordinal
13
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Yutaka Sakurai
series ordinal
14
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Shigeaki Nonoyama
series ordinal
15
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Yoshikatsu Kanai
series ordinal
16
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Nariyoshi Shinomiya
series ordinal
17
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language of work or name
English
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publication date
December 2008
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published in
American Journal of Human Genetics
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volume
83
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issue
6
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page(s)
744-51
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cites work
SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout
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Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder
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retrieved
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based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1016/J.AJHG.2008.11.001
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1623847
Fatcat ID
release_n6ucg4sihvgctegxxwidiqpzma
1 reference
stated in
Fatcat
reference URL
https://api.fatcat.wiki/v0/release/n6ucg4sihvgctegxxwidiqpzma
retrieved
24 November 2022
based on heuristic
mapped directly with Wikidata item
OpenCitations bibliographic resource ID
1623847
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1623847
PMC publication ID
2668068
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1623847
PubMed publication ID
19026395
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1623847
ResearchGate publication ID
23490308
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