{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Comegna M"],"funding":["Regione Campania"],"pagination":["2451-2456"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC6293129"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["6(12)"],"pubmed_abstract":["Microvillous inclusion disease (MVID) typically appears with severe chronic diarrhea in the few days after birth and rapidly causes dehydration and metabolic acidosis. In this context, presenting two novel cases, we underline the crucial importance of mutation analysis for the diagnosis of this disease that may be easily misdiagnosed."],"journal":["Clinical case reports"],"pubmed_title":["Two cases of microvillous inclusion disease caused by novel mutations in <i>MYO5B</i> gene."],"pmcid":["PMC6293129"],"funding_grant_id":["DGRC 1901/09"],"pubmed_authors":["Morroni M","Amato F","Comegna M","Spagnuolo MI","Guarino A","Liguori R","Castaldo G","Berni Canani R"],"additional_accession":[]},"is_claimable":false,"name":"Two cases of microvillous inclusion disease caused by novel mutations in <i>MYO5B</i> gene.","description":"Microvillous inclusion disease (MVID) typically appears with severe chronic diarrhea in the few days after birth and rapidly causes dehydration and metabolic acidosis. In this context, presenting two novel cases, we underline the crucial importance of mutation analysis for the diagnosis of this disease that may be easily misdiagnosed.","dates":{"release":"2018-01-01T00:00:00Z","publication":"2018 Dec","modification":"2024-11-08T18:58:52.747Z","creation":"2019-03-27T00:13:14Z"},"accession":"S-EPMC6293129","cross_references":{"pubmed":["30564347"],"doi":["10.1002/ccr3.1879"]}}