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Novel missense mutations of SAR1B gene in an infant with chylomicron retention disease

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dc.contributor.authorSuporn Treepongkarunaen_US
dc.contributor.authorNalinee Chongviriyaphanen_US
dc.contributor.authorUmaporn Suthutvoravuten_US
dc.contributor.authorDussadee Charoenpipopen_US
dc.contributor.authorLulin Choubtumen_US
dc.contributor.authorDuangrurdee Wattanasirichaigoonen_US
dc.contributor.otherFaculty of Medicine, Ramathibodi Hospital, Mahidol Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-09-13T07:04:14Z
dc.date.available2018-09-13T07:04:14Z
dc.date.issued2009-03-01en_US
dc.identifier.citationJournal of Pediatric Gastroenterology and Nutrition. Vol.48, No.3 (2009), 370-373en_US
dc.identifier.doi10.1097/MPG.0b013e318183188fen_US
dc.identifier.issn02772116en_US
dc.identifier.other2-s2.0-67650382105en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/28162
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67650382105&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleNovel missense mutations of SAR1B gene in an infant with chylomicron retention diseaseen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67650382105&origin=inwarden_US

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