Rare phenotype of ALS4 associated with heterozygous missense mutation c.5842A > G/p.M1948V in helicase domain of SETX gene. Issue 3 (2nd April 2020)

Record Type:: Journal Article
Title:: Rare phenotype of ALS4 associated with heterozygous missense mutation c.5842A > G/p.M1948V in helicase domain of SETX gene. Issue 3 (2nd April 2020)
Main Title:: Rare phenotype of ALS4 associated with heterozygous missense mutation c.5842A > G/p.M1948V in helicase domain of SETX gene
Authors:: Andreini, I.
Moro, F.
Africa, L.M.
Rubegni, A.
Santorelli, F.M.
Scarpini, C.
Sicurelli, F.
Battisti, C.
Abstract:
Is Part Of:: Amyotrophic lateral sclerosis and frontotemporal degeneration. Volume 21:Issue 3/4(2020)
Journal:: Amyotrophic lateral sclerosis and frontotemporal degeneration
Issue:: Volume 21:Issue 3/4(2020)
Issue Display:: Volume 21, Issue 3/4 (2020)
Year:: 2020
Volume:: 21
Issue:: 3/4
Issue Sort Value:: 2020-0021-NaN-0000
Page Start:: 312
Page End:: 313
Publication Date:: 2020-04-02
Subjects:: 616.839
Journal URLs:: http://informahealthcare.com/journal/afd ↗
http://informahealthcare.com ↗
DOI:: 10.1080/21678421.2020.1740271 ↗
Languages:: English
ISSNs:: 2167-8421
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 0859.841188
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 13716.xml