Publication Name	World Journal of Gastroenterology
Manuscript ID	4602
Country	Thailand

Received	2013-07-10 09:45
Peer-Review Started	2013-07-10 10:21
First Decision by Editorial Office Director
Return for Revision	2013-07-29 11:36
Revised	2013-08-29 17:14
Publication Fee Transferred
Second Decision by Editor	2013-09-17 09:49
Second Decision by Editor-in-Chief
Final Decision by Editorial Office Director	2013-09-17 11:33
Articles in Press
Edit the Manuscript by Language Editor	2013-10-16 23:26
Typeset the Manuscript	2013-11-26 10:26
Publish the Manuscript Online	2013-12-18 09:53

ISSN	1007-9327 (print) and 2219-2840 (online)
Open Access
Copyright
Article Reprints	For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
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Publisher	Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website	http://www.wjgnet.com

Category	Genetics & Heredity
Manuscript Type	Autobiography
Article Title	Screening of SLC25A13 mutation in the Thai population
Manuscript Source	Invited Manuscript
All Author List	Parith Wongkittichote, Chonlaphat Sukasem, Atsuo Kikuchi, Wichai Aekplakorn, Laran T Jensen, Shigeo Kure and Duangrurdee Wattanasirichaigoon
Funding Agency and Grant Number	Funding Agency Grant Number Mahidol University Faculty of Science and Ramathibodi Hospital Faculty of Medicine to Jensen LT and Wattanasirichaigoon D Mahidol University 49/2556 (Wattanasirichaigoon D) Pharmacogenomics Project, the collaborative project from the Thailand Center of Excellence for Life Science and Mahidol University to Sukasem C Medical Scholars Program of Mahidol University to Wongkittichote P Faculty of Medicine Ramathibodi Hospital to Wattanasirichaigoon D
Corresponding Author	Duangrurdee Wattanasirichaigoon, MD, Professor of Pediatrics, Division of Medical Genetics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand. duangrurdee.wat@mahidol.ac.th
Key Words	Aspartate-glutamate carrier; Isoform 2; Citrin deficiency; Type Ⅱ citrullinemia; Neonatal intrahepatic cholestasis caused by citrin deficiency; SLC25A13
Core Tip	Citrin deficiency is underestimated in various populations and the high prevalence of some SLC25A13 variants possibly contribute to uncharacterized predisposition/protection of certain disorders.
Publish Date	2013-12-18 09:53
Citation	Wongkittichote P, Sukasem C, Kikuchi A, Aekplakorn W, Jensen LT, Kure S, Wattanasirichaigoon D. Screening of SLC25A13 mutation in the Thai population. World J Gastroenterol 2013; 19(43): 7735-7742
URL	http://www.wjgnet.com/1007-9327/full/v19/i43/7735.htm
DOI	http://dx.doi.org/10.3748/wjg.v19.i43.7735

Full Article (PDF)	WJG-19-7735.pdf
Manuscript File	4602-Review.docx
Answering Reviewers	4602-Answering reviewers.pdf
Copyright License Agreement	4602-Copyright assignment.pdf
Non-Native Speakers of English Editing Certificate	4602-Language certificate.pdf
Peer-review Report	4602-Peer reviews.pdf
Scientific Editor Work List	4602-Scientific editor work list.doc