Case Report
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World J Gastrointest Pharmacol Ther. Oct 6, 2011; 2(5): 42-45
Published online Oct 6, 2011. doi: 10.4292/wjgpt.v2.i5.42
Contribution of G71R mutation to Gilbert’s syndrome phenotype in a Greek patient: A case report
Vassiliki Kalotychou, Maria Karakosta, Revekka Tzanetea, Aleka Stamoulakatou, Kostas Konstantopoulos, Yannis Rombos
Vassiliki Kalotychou, Maria Karakosta, Revekka Tzanetea, Kostas Konstantopoulos, Yannis Rombos, 1st Department of Internal Medicine, University of Athens, Athens, 11527, Greece
Aleka Stamoulakatou, Childrens’ Hospital “Aghia Sophia”, Athens, 11527, Greece
Author contributions: Kalotychou V performed research, reviewed the literature and wrote the final draft of the paper; Karakosta M performed research; Tzanetea R participated in writing the manuscript; Stamoulakatou A was the referring physician of the clinical case; Konstantopoulos K critically reviewed the manuscript; Rombos Y critically reviewed the manuscript and approved the final version.
Supported by Research Committee Special Account (ELKE)
Correspondence to: Vassiliki Kalotychou, PhD, 1st Department of Internal Medicine, University of Athens, “Laikon” Hospital, 17 Agiou Thoma str, Athens, 11527, Greece. vkalotyc@med.uoa.gr
Telephone: +30-210-7462511 Fax: +30-210-7788830
Received: May 17, 2011
Revised: September 20, 2011
Accepted: September 28, 2011
Published online: October 6, 2011
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