A Novel Mutation of Human Liver Alanine:Glyoxylate Aminotransferase Causes Primary Hyperoxaluria Type 1

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Veröffentlicht in:Acta histochemica et cytochemica 2012-03, Vol.45 (2), p.121
Hauptverfasser: Kawai, Chikage, Minatogawa, Yohsuke, Akiyoshi, Hidetaka, Hirose, Shinichi, Suehiro, Tsunatoshi, Tone, Shigenobu
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container_issue 2
container_start_page 121
container_title Acta histochemica et cytochemica
container_volume 45
creator Kawai, Chikage
Minatogawa, Yohsuke
Akiyoshi, Hidetaka
Hirose, Shinichi
Suehiro, Tsunatoshi
Tone, Shigenobu
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source Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese; PubMed Central; Free Full-Text Journals in Chemistry
title A Novel Mutation of Human Liver Alanine:Glyoxylate Aminotransferase Causes Primary Hyperoxaluria Type 1
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