Extending the clinical phenotype associated with biallelic NTHL1 germline mutations. Issue 6 (24th September 2018)

Record Type:: Journal Article
Title:: Extending the clinical phenotype associated with biallelic NTHL1 germline mutations. Issue 6 (24th September 2018)
Main Title:: Extending the clinical phenotype associated with biallelic NTHL1 germline mutations
Authors:: Fostira, Florentia
Kontopodis, Emmanouil
Apostolou, Paraskevi
Fragkaki, Maria
Androulakis, Nikolaos
Yannoukakos, Drakoulis
Konstantopoulou, Irene
Saloustros, Emmanouil
Abstract:: Abstract :
Is Part Of:: Clinical genetics. Volume 94:Issue 6(2018)
Journal:: Clinical genetics
Issue:: Volume 94:Issue 6(2018)
Issue Display:: Volume 94, Issue 6 (2018)
Year:: 2018
Volume:: 94
Issue:: 6
Issue Sort Value:: 2018-0094-0006-0000
Page Start:: 588
Page End:: 589
Publication Date:: 2018-09-24
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.13444 ↗
Languages:: English
ISSNs:: 0009-9163
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3286.287000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 14169.xml