Atypical phenotype? The answer's in the genotype: AGS caused by a novel RNASEH2C variant combined with XLA caused by a BTK deficiency. (20th January 2021)

Record Type:: Journal Article
Title:: Atypical phenotype? The answer's in the genotype: AGS caused by a novel RNASEH2C variant combined with XLA caused by a BTK deficiency. (20th January 2021)
Main Title:: Atypical phenotype? The answer's in the genotype: AGS caused by a novel RNASEH2C variant combined with XLA caused by a BTK deficiency
Authors:: Boulanger, Cécile
Chatzis, Olga
Nolf, Delphine
Brichard, Bénédicte
Lauwerys, Bernard
Nassogne, Marie-Cécile
Limaye, Nisha
Abstract:
Is Part Of:: Rheumatology. Volume 60:Number 7(2021)
Journal:: Rheumatology
Issue:: Volume 60:Number 7(2021)
Issue Display:: Volume 60, Issue 7 (2021)
Year:: 2021
Volume:: 60
Issue:: 7
Issue Sort Value:: 2021-0060-0007-0000
Page Start:: e240
Page End:: e242
Publication Date:: 2021-01-20
Subjects:: Rheumatism -- Periodicals
Rheumatology -- Periodicals
616.723005
Journal URLs:: http://rheumatology.oupjournals.org ↗
http://rheumatology.oxfordjournals.org ↗
http://ukcatalogue.oup.com/ ↗
http://firstsearch.oclc.org ↗
DOI:: 10.1093/rheumatology/keab051 ↗
Languages:: English
ISSNs:: 1462-0324
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 7960.731900
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Ingest File:: 24939.xml