First replication that biallelic variants in FITM2 cause a complex deafness‐dystonia syndrome. Issue 10 (4th October 2018)

Record Type:: Journal Article
Title:: First replication that biallelic variants in FITM2 cause a complex deafness‐dystonia syndrome. Issue 10 (4th October 2018)
Main Title:: First replication that biallelic variants in FITM2 cause a complex deafness‐dystonia syndrome
Authors:: Riedhammer, Korbinian Maria
Leszinski, Gloria Sarah
Andres, Stephanie
Strobl‐Wildemann, Gertrud
Wagner, Matias
Abstract:
Is Part Of:: Movement disorders. Volume 33:Issue 10(2018)
Journal:: Movement disorders
Issue:: Volume 33:Issue 10(2018)
Issue Display:: Volume 33, Issue 10 (2018)
Year:: 2018
Volume:: 33
Issue:: 10
Issue Sort Value:: 2018-0033-0010-0000
Page Start:: 1665
Page End:: 1666
Publication Date:: 2018-10-04
Subjects:: FITM2 -- dystonia -- deafness -- hyperkeratosis -- exome
Movement disorders -- Periodicals
610
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1531-8257 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/mds.27481 ↗
Languages:: English
ISSNs:: 0885-3185
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 5980.317200
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 8386.xml