Show simple item record

NOVEL MUTATIONS IN GENES CAUSING CHARCOT-MARIE-TOOTH NEUROPATHY AND HEREDITARY SPASTIC PARAPLEGIA IDENTIFIED BY HOMWES

dc.contributor.authorBattaloglu, E.
dc.contributor.authorParman, Y.
dc.contributor.authorTourney, I
dc.contributor.authorEstrada-Cuzcano, A.
dc.contributor.authorJordanova, A.
dc.contributor.authorAtkinson, D.
dc.contributor.authorKancheva, D.
dc.contributor.authorZimon, M.
dc.contributor.authorDe Rijk, P.
dc.contributor.authorChamova, T.
dc.contributor.authorMitev, V
dc.contributor.authorFabrizi, G. M.
dc.contributor.authorTopaloglu, H.
dc.date.accessioned2021-03-04T11:50:44Z
dc.date.available2021-03-04T11:50:44Z
dc.identifier.citationAtkinson D., Kancheva D., Zimon M., De Rijk P., Chamova T., Mitev V., Fabrizi G. M. , Topaloglu H., Tourney I., Parman Y., et al., "NOVEL MUTATIONS IN GENES CAUSING CHARCOT-MARIE-TOOTH NEUROPATHY AND HEREDITARY SPASTIC PARAPLEGIA IDENTIFIED BY HOMWES", Biennial Meeting of the Peripheral-Nerve-Society, Quebec, Kanada, 27 Haziran - 02 Temmuz 2015, cilt.20, ss.98
dc.identifier.othervv_1032021
dc.identifier.otherav_746289d7-bb3b-4df0-ba86-7ee3476ae45d
dc.identifier.urihttp://hdl.handle.net/20.500.12627/79997
dc.language.isoeng
dc.subjectSinirbilim ve Davranış
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectYaşam Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectTemel Bilimler
dc.subjectNEUROSCIENCES
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleNOVEL MUTATIONS IN GENES CAUSING CHARCOT-MARIE-TOOTH NEUROPATHY AND HEREDITARY SPASTIC PARAPLEGIA IDENTIFIED BY HOMWES
dc.typeBildiri
dc.contributor.departmentVIB Antwerp , ,
dc.identifier.volume20
dc.contributor.firstauthorID147151


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record