Analysis of large-scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemia.

2.50
Hdl Handle:
http://hdl.handle.net/11287/620407
Title:
Analysis of large-scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemia.
Authors:
Laver, T. W.; Weedon, M. N.; Caswell, R.; Hussain, K.; Ellard, Sian ( 0000-0002-7620-5526 ) ; Flanagan, S. E.
Citation:
Analysis of large-scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemia. 2017, 38 (10):1442-1444 Hum. Mutat.
Publisher:
Wiley
Journal:
Human Mutation
Issue Date:
Oct-2017
URI:
http://hdl.handle.net/11287/620407
DOI:
10.1002/humu.23289
PubMed ID:
28681398
Additional Links:
http://dx.doi.org/10.1002/humu.23289
Type:
Letter
Language:
en
ISSN:
1098-1004
Appears in Collections:
Molecular Genetics; 2017 RD&E publications

Full metadata record

DC FieldValue Language
dc.contributor.authorLaver, T. W.en
dc.contributor.authorWeedon, M. N.en
dc.contributor.authorCaswell, R.en
dc.contributor.authorHussain, K.en
dc.contributor.authorEllard, Sianen
dc.contributor.authorFlanagan, S. E.en
dc.date.accessioned2017-09-19T10:05:21Z-
dc.date.available2017-09-19T10:05:21Z-
dc.date.issued2017-10-
dc.identifier.citationAnalysis of large-scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemia. 2017, 38 (10):1442-1444 Hum. Mutat.en
dc.identifier.issn1098-1004-
dc.identifier.pmid28681398-
dc.identifier.doi10.1002/humu.23289-
dc.identifier.urihttp://hdl.handle.net/11287/620407-
dc.language.isoenen
dc.publisherWileyen
dc.relation.urlhttp://dx.doi.org/10.1002/humu.23289en
dc.rightsArchived with thanks to Human Mutationen
dc.subjectWessex Classification Subject Headings::Oncology. Pathology.::Geneticsen
dc.titleAnalysis of large-scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemia.en
dc.typeLetteren
dc.identifier.journalHuman Mutationen
dc.type.versionPublisheden

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